Canonical Allele Identifier: PA2826624871
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 630831
ClinVar RCV Id: RCV000776835 RCV000815193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser108Cys
CA346739996
NM_001281492.2:c.323C>G