Canonical Allele Identifier: PA2826631540
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 848664
ClinVar RCV Id: RCV001052471 RCV002445279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Cys477Tyr
CA346753398
NM_001281493.2:c.1430G>A