Allele Registry

Canonical Allele Identifier: PA125185

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016611

RCV000016612

ClinVar Variation:

15361

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu29Gln	CA125184 NM_000518.5:c.86T>A