Canonical Allele Identifier: PA658680969
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455197
ClinVar RCV Id: RCV000547711 RCV002282203 RCV001015434
ClinVar Variation Id: 1790838
ClinVar RCV Id: RCV002450307 RCV003759733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp803Glu
CA346753963
NM_000179.3:c.2409C>A
CA346753965
NM_000179.3:c.2409C>G