Canonical Allele Identifier: PA916011328
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 126892
ClinVar RCV Id: RCV000114751 RCV000223291 RCV001216258 RCV003453034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala925Pro
CA011702
NM_001281492.2:c.2773G>C