Allele Registry

Canonical Allele Identifier: PA2579933069

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000637303

RCV002358789

ClinVar Variation:

531190

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Leu133Phe	CA5779321 NM_001130442.3:c.397C>T