Canonical Allele Identifier: PA2826631515
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_001268422.1:p.Leu472Pro
CA346753216
NM_001281493.2:c.1415T>C