Allele Registry

Canonical Allele Identifier: PA2741816157

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV003324391

ClinVar Variation:

2577314

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala87Ser	CA379273807 NM_000518.5:c.259G>T