Allele Registry

Canonical Allele Identifier: PA124866

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016354

RCV000016355

ClinVar Variation:

15177

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asn81Lys	CA124865 NM_000518.5:c.243C>A CA217113806 NM_000518.5:c.243C>G