Canonical Allele Identifier: PA2826626835
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 928260
ClinVar RCV Id: RCV001192034 RCV003462666 RCV004010566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu565Val
CA346750829
NM_001281492.2:c.1693C>G