Allele Registry

Canonical Allele Identifier: PA124952

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016417

RCV000985739

ClinVar Variation:

15221

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His78Asp	CA124951 NM_000518.5:c.232C>G