Allele Registry

Canonical Allele Identifier: PA124954

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016418

RCV001284633

ClinVar Variation:

15222

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys60Thr	CA124953 NM_000518.5:c.179A>C