Allele Registry

Canonical Allele Identifier: PA125423

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016811

RCV003234910

ClinVar Variation:

15545

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala141Val	CA125422 NM_000518.5:c.422C>T