Allele Registry

Canonical Allele Identifier: PA124751

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016266

ClinVar Variation:

15111

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asn103Ser	CA124750 NM_000518.5:c.308A>G