Allele Registry

Canonical Allele Identifier: PA125157

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016590

ClinVar Variation:

15347

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Phe43Val	CA125156 NM_000518.5:c.127T>G