Canonical Allele Identifier: PA2825089359
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788028
ClinVar RCV Id: RCV002428173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu743Trp
CA346752486
NM_000179.3:c.2228T>G