Allele Registry

Canonical Allele Identifier: PA124946

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016414

ClinVar Variation:

15218

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys96Met	CA124945 NM_000518.5:c.287A>T