Allele Registry

Canonical Allele Identifier: PA124755

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016268

ClinVar Variation:

15113

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His64Pro	CA124754 NM_000518.5:c.191A>C