Allele Registry

Canonical Allele Identifier: PA124968

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016427

ClinVar Variation:

15229

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys121Ile	CA124967 NM_000518.5:c.362A>T