Canonical Allele Identifier: PA2499265639
Gene: B2M HGNC NCBI

Linked Data

ClinVar Variation Id: 1011724
ClinVar RCV Id: RCV001309565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004039.1:p.Arg3Cys
CA7536257
NM_004048.4:c.7C>T