Canonical Allele Identifier: PA330395
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89236
ClinVar RCV Id: RCV001357734 RCV003593868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser666Pro
CA009527
NM_000179.3:c.1996T>C