Canonical Allele Identifier: PA2825086619
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1520225
ClinVar RCV Id: RCV002038581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser227Arg
CA346739870
NM_000179.3:c.679A>C
CA346739883
NM_000179.3:c.681T>A
CA346739887
NM_000179.3:c.681T>G