Canonical Allele Identifier: PA2826628394
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 857589
ClinVar RCV Id: RCV001063296 RCV002451272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg1015Lys
CA346758965
NM_001281492.2:c.3044G>A