Canonical Allele Identifier: PA645382035
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410458
ClinVar RCV Id: RCV002230112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala787Gly
CA16611147
NM_000179.3:c.2360C>G