Allele Registry

Canonical Allele Identifier: PA125055

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016514

ClinVar Variation:

15284

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Tyr131Ser	CA125054 NM_000518.5:c.392A>C