Canonical Allele Identifier: PA2826465538
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790666
ClinVar RCV Id: RCV002450225 RCV003101788 RCV003455467 RCV004007426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu734Pro
CA346730184
NM_001258281.1:c.2201T>C