Canonical Allele Identifier: PA335868
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216316
ClinVar RCV Id: RCV002229121 RCV002453725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His1207Tyr
CA335866
NM_000179.3:c.3619C>T