Canonical Allele Identifier: PA2826627287
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418961
ClinVar RCV Id: RCV000481034 RCV000528139 RCV000572051 RCV000781592 RCV001140446 RCV003463987 RCV004002280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys674Glu
CA16617672
NM_001281492.2:c.2020A>G