Allele Registry

Canonical Allele Identifier: PA124790

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016297

RCV000641428

ClinVar Variation:

15134

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asp100Val	CA124789 NM_000518.5:c.299A>T