Allele Registry

Canonical Allele Identifier: PA125035

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016496

ClinVar Variation:

15270

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val24Gly	CA125034 NM_000518.5:c.71T>G