Allele Registry

Canonical Allele Identifier: PA125140

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016581

RCV000508375

ClinVar Variation:

15338

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Leu92Pro	CA125139 NM_000518.5:c.275T>C