Canonical Allele Identifier: PA2499247998
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1055387
ClinVar RCV Id: RCV001364047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Asn93Ser
CA216881989
NM_001318054.2:c.278A>G