Canonical Allele Identifier: PA913192152
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 630731
ClinVar RCV Id: RCV000776701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu979Val
CA346756210
NM_000179.3:c.2935C>G