Allele Registry

Canonical Allele Identifier: PA124988

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016443

RCV000016446

RCV001811157

RCV001826464

ClinVar Variation:

15241

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val99Met	CA124987 NM_000518.5:c.295G>A