Canonical Allele Identifier: PA658680854
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485882
ClinVar RCV Id: RCV000561723 RCV001299179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser722Cys
CA346751157
NM_000179.3:c.2165C>G