Canonical Allele Identifier: PA645468367
Gene: B2M HGNC NCBI

Linked Data

ClinVar Variation Id: 376371
ClinVar RCV Id: RCV000419044 RCV000419253 RCV000420355 RCV000427508 RCV000429996 RCV000426708 RCV000437364 RCV000439772 RCV000444855 RCV000438190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004039.1:p.Met1Thr