Allele Registry

Canonical Allele Identifier: PA124925

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016392

RCV000016393

ClinVar Variation:

15207

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Cys113Arg	CA124924 NM_000518.5:c.337T>C