Canonical Allele Identifier: PA2825092319
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 824242
ClinVar RCV Id: RCV001021196 RCV001861011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Cys1269Tyr
CA346761219
NM_000179.3:c.3806G>A