Allele Registry

Canonical Allele Identifier: PA124876

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016360

RCV000016361

ClinVar Variation:

15182

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asn140Asp	CA124875 NM_000518.5:c.418A>G