Canonical Allele Identifier: PA2826627644
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 41591
ClinVar RCV Id: RCV000034496 RCV000115393 RCV000235185 RCV000410628 RCV001080247 RCV003492327
ClinVar Variation Id: 2698505
ClinVar RCV Id: RCV003594839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gln759His
CA010704
NM_001281492.2:c.2277G>T
CA346755231
NM_001281492.2:c.2277G>C