Allele Registry

Canonical Allele Identifier: PA2573100328

Gene: HRAS HGNC NCBI

ClinVar Allele:

1325102

ClinVar RCV:

RCV001813657

RCV002541490

ClinVar Variation:

1334242

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Ala59Ser	CA378924686 NM_176795.5:c.175G>T