Allele Registry

Canonical Allele Identifier: PA125477

Gene: HBB HGNC NCBI

ClinVar Allele:

30615

ClinVar RCV:

RCV000016843

ClinVar Variation:

15576

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys145Met	CA125476 NM_000518.5:c.434A>T