Canonical Allele Identifier: PA2826627367
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230532
ClinVar RCV Id: RCV004520683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu692Arg
CA346754100
NM_001281492.2:c.2075T>G