Allele Registry

Canonical Allele Identifier: PA125510

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016865

ClinVar Variation:

15598

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Phe42Cys	CA125509 NM_000518.5:c.125T>G