Canonical Allele Identifier: PA169171
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142698
ClinVar RCV Id: RCV000132064 RCV000230863 RCV000589862 RCV000758606 RCV001420719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg361Cys
CA007972
NM_000179.3:c.1081C>T