Canonical Allele Identifier: PA2826625228
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1767599
ClinVar RCV Id: RCV002376470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser191Ala
CA346740905
NM_001281492.2:c.571T>G