Allele Registry

Canonical Allele Identifier: PA124932

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016398

ClinVar Variation:

15211

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys66Met	CA124931 NM_000518.5:c.197A>T