Canonical Allele Identifier: PA2825090078
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1795748
ClinVar RCV Id: RCV002439558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys923Gln
CA346755450
NM_000179.3:c.2767A>C