Canonical Allele Identifier: PA2826633569
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428361
ClinVar RCV Id: RCV000491034 RCV000664316 RCV002523440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Cys939Tyr
CA46719383
NM_001281493.2:c.2816G>A