Canonical Allele Identifier: PA2825088103
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1770363
ClinVar RCV Id: RCV002387711 RCV003759668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu447Pro
CA346744585
NM_000179.3:c.1340T>C