Canonical Allele Identifier: PA2830359835
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12611
ClinVar RCV Id: RCV000013445 RCV000419902 RCV000436710 RCV000427529 RCV000426668 RCV000436017 RCV000444744
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Ala146Val
CA256494
NM_176795.5:c.437C>T