Canonical Allele Identifier: PA2579931723
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 936794
ClinVar RCV Id: RCV001205671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ala155Ser
CA378921217
NM_001130442.3:c.463G>T