Canonical Allele Identifier: PA2826624892
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182611
ClinVar RCV Id: RCV000160655 RCV000459365 RCV000568587 RCV001030489 RCV001270441 RCV003462092 RCV003230421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg113His
CA016346
NM_001281492.2:c.338G>A