Canonical Allele Identifier: PA2825086126
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453181
ClinVar RCV Id: RCV003182636 RCV003779572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser137Cys
CA346737111
NM_000179.3:c.409A>T