Canonical Allele Identifier: PA2826626637
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455166
ClinVar RCV Id: RCV000570350 RCV000558083 RCV004003667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly522Trp
CA346750566
NM_001281492.2:c.1564G>T