Allele Registry

Canonical Allele Identifier: PA2573062958

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV001811763

ClinVar Variation:

1330628

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp74His	CA379273847 NM_000518.5:c.220G>C