Canonical Allele Identifier: PA2826626329
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1779231
ClinVar RCV Id: RCV002407494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg451Ser
CA346748880
NM_001281492.2:c.1353A>C
CA346748881
NM_001281492.2:c.1353A>T