Allele Registry

Canonical Allele Identifier: PA125445

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016824

ClinVar Variation:

15558

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val2Leu	CA125444 NM_000518.5:c.4G>T CA379275042 NM_000518.5:c.4G>C