Canonical Allele Identifier: PA2826463465
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182555
ClinVar RCV Id: RCV000160578 RCV000203837 RCV002444666 RCV003467247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met234Val
CA022496
NM_001258281.1:c.700A>G