Allele Registry

Canonical Allele Identifier: PA125508

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016864

ClinVar Variation:

15597

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val127Leu	CA125507 NM_000518.5:c.379G>C CA379273693 NM_000518.5:c.379G>T