Canonical Allele Identifier: PA915965021
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821109
ClinVar RCV Id: RCV001015208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Trp777Gly
CA346753329
NM_000179.3:c.2329T>G