Canonical Allele Identifier: PA2825086137
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1738316
ClinVar RCV Id: RCV002333295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr139Pro
CA346737123
NM_000179.3:c.415A>C