Canonical Allele Identifier: PA2826463331
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2014435
ClinVar RCV Id: RCV002830033 RCV004064959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val201Phe
CA346732747
NM_001258281.1:c.601G>T