Allele Registry

Canonical Allele Identifier: PA124837

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016328

ClinVar Variation:

15160

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala63Pro	CA124836 NM_000518.5:c.187G>C