Canonical Allele Identifier: PA2826465710
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2831992
ClinVar RCV Id: RCV003758288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys781Asn
CA346730837
NM_001258281.1:c.2343A>C
CA346730839
NM_001258281.1:c.2343A>T