Canonical Allele Identifier: PA2826466031
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413129
ClinVar RCV Id: RCV001943368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile860Leu
CA346732147
NM_001258281.1:c.2578A>C