Allele Registry

Canonical Allele Identifier: PA2579931912

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000434487

RCV000637302

ClinVar Variation:

40445

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Asp154Asn	CA5779226 NM_001130442.3:c.460G>A