Allele Registry

Canonical Allele Identifier: PA2579931333

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000494039

RCV000705122

ClinVar Variation:

430506

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Lys101Arg	CA378923959 NM_001130442.3:c.302A>G