Canonical Allele Identifier: PA2826625225
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1049063
ClinVar RCV Id: RCV001354669 RCV002384495 RCV003738052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro190Thr
CA073647
NM_001281492.2:c.568C>A