Canonical Allele Identifier: PA2826463346
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455615
ClinVar RCV Id: RCV000544343 RCV001764526 RCV002289719 RCV004023722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu204Val
CA040694
NM_001258281.1:c.610C>G