Canonical Allele Identifier: PA2826465519
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790465
ClinVar RCV Id: RCV002457918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro729Ser
CA346730119
NM_001258281.1:c.2185C>T