Canonical Allele Identifier: PA1139699175
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 936794
ClinVar RCV Id: RCV001205671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Ala76Ser
CA378921217
NM_001318054.2:c.226G>T