Allele Registry

Canonical Allele Identifier: PA2579932271

Gene: HRAS HGNC NCBI

ClinVar Allele:

1030305

ClinVar RCV:

RCV001347584

ClinVar Variation:

1043469

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Thr87Ile	CA378924419 NM_001130442.3:c.260C>T