Allele Registry

Canonical Allele Identifier: PA3063016448

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV005432030

ClinVar Variation:

3907482

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly25Ser	CA379274801 NM_000518.5:c.73G>A