Canonical Allele Identifier: PA891846080
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 577488
ClinVar RCV Id: RCV000700261 RCV001798963 RCV002369920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly308Ser
CA46706999
NM_000179.3:c.922G>A