Allele Registry

Canonical Allele Identifier: PA124956

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016420

ClinVar Variation:

15223

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala14Asp	CA124955 NM_000518.5:c.41C>A