Canonical Allele Identifier: PA2826634641
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_001268423.1:p.Leu145Pro
CA346744585
NM_001281494.2:c.434T>C