Canonical Allele Identifier: PA2826463222
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2120960
ClinVar RCV Id: RCV003025353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn176Thr
CA346732162
NM_001258281.1:c.527A>C