Allele Registry

Canonical Allele Identifier: PA124880

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016364

RCV003441719

ClinVar Variation:

15184

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala28Val	CA124879 NM_000518.5:c.83C>T