Canonical Allele Identifier: PA2826627658
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1900392
ClinVar RCV Id: RCV002576489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser762Tyr
CA346755265
NM_001281492.2:c.2285C>A