Canonical Allele Identifier: PA2826625255
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184803
ClinVar RCV Id: RCV000164123 RCV000204780 RCV000479969 RCV003150013 RCV003137692 RCV003995316 RCV004528909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr197Ser
CA016745
NM_001281492.2:c.590C>G
CA346741015
NM_001281492.2:c.589A>T