Allele Registry

Canonical Allele Identifier: PA125067

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016521

ClinVar Variation:

15290

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val135Glu	CA125066 NM_000518.5:c.404T>A