Canonical Allele Identifier: PA2826635778
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1971951
ClinVar RCV Id: RCV002745826 RCV004017947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp411Tyr
CA346751060
NM_001281494.2:c.1231G>T