Allele Registry

Canonical Allele Identifier: PA124950

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016416

ClinVar Variation:

15220

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala129Asp	CA124949 NM_000518.5:c.386C>A