Allele Registry

Canonical Allele Identifier: PA125200

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016622

ClinVar Variation:

15370

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys121Gln	CA125199 NM_000518.5:c.361A>C