Canonical Allele Identifier: PA2825089477
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2805245
ClinVar RCV Id: RCV003760731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu774Pro
CA346753216
NM_000179.3:c.2321T>C