Canonical Allele Identifier: PA645468362
Gene: B2M HGNC NCBI

Linked Data

ClinVar Variation Id: 376369
ClinVar RCV Id: RCV000419609 RCV000424715 RCV000417544 RCV000420829 RCV000430542 RCV000424903 RCV000435632 RCV000438049 RCV000441263 RCV000445210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004039.1:p.Met1Val