Allele Registry

Canonical Allele Identifier: PA658828623

Gene: HRAS HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000148033

RCV000157918

RCV000418005

RCV000418550

RCV000435225

RCV000437086

RCV000662268

RCV001813393

RCV001844808

ClinVar Variation:

160364

376320

376321

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Gln61Arg	CA173968 NM_176795.5:c.182A>G CA16602766 NM_176795.5:c.182_183delinsGT CA16602767 NM_176795.5:c.182_183delinsGA CA645569138 NM_176795.5:c.181_182delinsAG