Canonical Allele Identifier: PA2825091759
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015363
ClinVar RCV Id: RCV001314213 RCV001751602 RCV002456410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1182Thr
CA346760254
NM_000179.3:c.3545G>C