Canonical Allele Identifier: PA129892
Gene: B2M HGNC NCBI

Linked Data

ClinVar Variation Id: 31907
ClinVar RCV Id: RCV000024598 RCV000989305
JSON-LD

Amino-acid Alleles

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