Allele Registry

Canonical Allele Identifier: PA124928

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016396

ClinVar Variation:

15209

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His93Asp	CA124927 NM_000518.5:c.277C>G