Allele Registry

Canonical Allele Identifier: PA129892

Gene: B2M HGNC NCBI

ClinVar RCV:

RCV000024598

RCV000989305

ClinVar Variation:

31907

HGVS (amino-acid)	Matching Registered Transcripts
NP_004039.1:p.Asp96Asn	CA129891 NM_004048.4:c.286G>A