Canonical Allele Identifier: PA2826462785
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 662989
ClinVar RCV Id: RCV000820762 RCV003307549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn18Tyr
CA346729528
NM_001258281.1:c.52A>T