Canonical Allele Identifier: PA2825089569
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790403
ClinVar RCV Id: RCV002457857 RCV004007425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp793Glu
CA346753736
NM_000179.3:c.2379T>A
CA346753739
NM_000179.3:c.2379T>G