Allele Registry

Canonical Allele Identifier: PA124899

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016377

ClinVar Variation:

15194

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Glu27Val	CA124898 NM_000518.5:c.80A>T