Canonical Allele Identifier: PA2826631635
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455196
ClinVar RCV Id: RCV000527339 RCV002456040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp501Tyr
CA346753957
NM_001281493.2:c.1501G>T