Allele Registry

Canonical Allele Identifier: PA125218

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016631

ClinVar Variation:

15379

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Pro125Ser	CA125217 NM_000518.5:c.373C>T