Canonical Allele Identifier: PA2826637387
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 135841
ClinVar RCV Id: RCV000122963 RCV000128933 RCV000411062 RCV000587527 RCV001255217 RCV001354177 RCV003149837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro785Ala
CA012231
NM_001281494.2:c.2353C>G