Allele Registry

Canonical Allele Identifier: PA2579931345

Gene: HRAS HGNC NCBI

ClinVar Allele:

935599

ClinVar RCV:

RCV001204299

ClinVar Variation:

935657

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Lys88Arg	CA378924406 NM_001130442.3:c.263A>G