Canonical Allele Identifier: PA2826634703
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2162051
ClinVar RCV Id: RCV003078884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu161Lys
CA346745060
NM_001281494.2:c.481G>A