Allele Registry

Canonical Allele Identifier: PA124773

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016279

RCV003114195

ClinVar Variation:

15122

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Phe86Ser	CA124772 NM_000518.5:c.257T>C