Canonical Allele Identifier: PA2580532830
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2416915
ClinVar RCV Id: RCV003109166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Thr74Ala
CA378924589
NM_176795.5:c.220A>G