Canonical Allele Identifier: PA2573308927
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1478514
ClinVar RCV Id: RCV001974222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Asp57_Gln61dup
CA2573147056
NM_176795.5:c.171_185dup