Allele Registry

Canonical Allele Identifier: PA124831

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016325

RCV003476893

ClinVar Variation:

15157

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys96Asn	CA124830 NM_000518.5:c.288G>C CA217113555 NM_000518.5:c.288G>T