Canonical Allele Identifier: PA2826625923
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1401433
ClinVar RCV Id: RCV001911806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu357Asp
CA346745791
NM_001281492.2:c.1071G>C
CA346745793
NM_001281492.2:c.1071G>T