Canonical Allele Identifier: PA1139674395
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 924411
ClinVar RCV Id: RCV001185701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu659Val
CA346750613
NM_000179.3:c.1975C>G