Canonical Allele Identifier: PA2825087108
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2133945
ClinVar RCV Id: RCV003044687 RCV004070114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly283dup
CA073501
NM_000179.3:c.848_850dup