Canonical Allele Identifier: PA645468372
Gene: B2M HGNC NCBI

Linked Data

ClinVar Variation Id: 376372
ClinVar RCV Id: RCV000421385 RCV000421129 RCV000428897 RCV000423518 RCV000432053 RCV000434386 RCV000434444 RCV000438363 RCV000439578 RCV000442386
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004039.1:p.Met1Arg