Canonical Allele Identifier: PA2826631653
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790981
ClinVar RCV Id: RCV002450382 RCV003759734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu505Gln
CA069001
NM_001281493.2:c.1513G>C