Allele Registry

Canonical Allele Identifier: PA125212

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016628

ClinVar Variation:

15376

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala143Pro	CA125211 NM_000518.5:c.427G>C