Canonical Allele Identifier: PA2826465961
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1795200
ClinVar RCV Id: RCV002431299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys841Asn
CA346731782
NM_001258281.1:c.2523G>C
CA346731784
NM_001258281.1:c.2523G>T