Allele Registry

Canonical Allele Identifier: PA2573062957

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV001801095

ClinVar Variation:

1330078

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp22Val	CA217115275 NM_000518.5:c.65A>T