Canonical Allele Identifier: PA2826626389
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525841
ClinVar RCV Id: RCV000630185 RCV004025378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu465Ser
CA346749252
NM_001281492.2:c.1394T>C