Allele Registry

Canonical Allele Identifier: PA125191

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016615

ClinVar Variation:

15364

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val68Ala	CA125190 NM_000518.5:c.203T>C