Allele Registry

Canonical Allele Identifier: PA645485982

Gene: NRAS HGNC NCBI

Linked Data

ClinVar RCV:

RCV000414646

RCV000418758

RCV000419887

RCV000420139

RCV000420910

RCV000422093

RCV000424220

RCV000426637

RCV000427364

RCV000428418

RCV000429512

RCV000429704

RCV000431603

RCV000434043

RCV000436751

RCV000436881

RCV000437158

RCV000438233

RCV000439006

RCV000439308

RCV000443672

RCV000444600

RCV001813470

ClinVar Variation:

373003

375871

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002515.1:p.Gln61His	CA16042285 NM_002524.5:c.183A>T CA16602358 NM_002524.5:c.183A>C