Allele Registry

Canonical Allele Identifier: PA124794

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016299

RCV001811148

ClinVar Variation:

15136

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys67Thr	CA124793 NM_000518.5:c.200A>C