Canonical Allele Identifier: PA916011325
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89342
ClinVar RCV Id: RCV000409200 RCV000218375 RCV000565213 RCV000627700 RCV000764427 RCV003460677 RCV003493433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala925Thr
CA011694
NM_001281492.2:c.2773G>A