Canonical Allele Identifier: PA192503
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185639
ClinVar RCV Id: RCV000165091
ClinVar Variation Id: 1365015
ClinVar RCV Id: RCV001907789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1304Ser
CA014672
NM_000179.3:c.3912G>T
CA346761443
NM_000179.3:c.3912G>C