Canonical Allele Identifier: PA915984268
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825021
ClinVar RCV Id: RCV001022744 RCV001066450 RCV004004631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser87Phe
CA346730512
NM_001258281.1:c.260C>T