Canonical Allele Identifier: PA2826464715
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90789
ClinVar RCV Id: RCV000811456 RCV002399464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala534Val
CA019334
NM_001258281.1:c.1601C>T