Canonical Allele Identifier: PA2742019207
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2885653
ClinVar RCV Id: RCV003626595

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Thr74Ser
CA378924586
NM_176795.5:c.221C>G
CA378924588
NM_176795.5:c.220A>T