Canonical Allele Identifier: PA2826636039
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216307
ClinVar RCV Id: RCV001190573 RCV001313045 RCV003454503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu471Pro
CA337352
NM_001281494.2:c.1412T>C