Canonical Allele Identifier: PA2826630708
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2084293
ClinVar RCV Id: RCV003011065 RCV004068428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Tyr287His
CA346749094
NM_001281493.2:c.859T>C