Allele Registry

Canonical Allele Identifier: PA125526

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016875

ClinVar Variation:

15608

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Phe104Val	CA125525 NM_000518.5:c.310T>G