Allele Registry

Canonical Allele Identifier: PA124769

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016276

RCV000016801

ClinVar Variation:

15536

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val68Met	CA124768 NM_000518.5:c.202G>A