Allele Registry

Canonical Allele Identifier: PA124741

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016260

RCV001284157

RCV001778654

ClinVar Variation:

15106

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val127Ala	CA124740 NM_000518.5:c.380T>C