Allele Registry

Canonical Allele Identifier: PA125380

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016781

ClinVar Variation:

15517

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val19Met	CA125379 NM_000518.5:c.55G>A