Canonical Allele Identifier: PA645468368
Gene: B2M HGNC NCBI

Linked Data

ClinVar Variation Id: 376370
ClinVar RCV Id: RCV000422880 RCV000421861 RCV000425118 RCV000430300 RCV000431428 RCV000432545 RCV000432685 RCV000441906 RCV000439880 RCV000440097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004039.1:p.Met1Leu