Canonical Allele Identifier: PA2826627947
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186374
ClinVar RCV Id: RCV000165958 RCV000214010 RCV000473325 RCV001526922 RCV003468765 RCV003995466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg829Cys
CA011024
NM_001281492.2:c.2485C>T