Canonical Allele Identifier: PA2826627376
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 838268
ClinVar RCV Id: RCV001039783 RCV003283880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile695Asn
CA346754138
NM_001281492.2:c.2084T>A