Canonical Allele Identifier: PA2826464047
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237365
ClinVar RCV Id: RCV000232170 RCV000573477 RCV000589179 RCV003998754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala368Val
CA027829
NM_001258281.1:c.1103C>T