Canonical Allele Identifier: PA2579923869
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073143
ClinVar RCV Id: RCV004015157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser900Pro
CA346731631
NM_000251.3:c.2698T>C