Allele Registry

Canonical Allele Identifier: PA125543

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016888

ClinVar Variation:

15621

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala71Val	CA125542 NM_000518.5:c.212C>T