Allele Registry

Canonical Allele Identifier: PA125025

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016488

ClinVar Variation:

15264

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Phe42Tyr	CA125024 NM_000518.5:c.125T>A