Canonical Allele Identifier: PA2826464137
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408536
ClinVar RCV Id: RCV000491177 RCV000467391 RCV001764410 RCV003463909 RCV004000792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile388Thr
CA16610869
NM_001258281.1:c.1163T>C