Canonical Allele Identifier: PA2826631170
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479902
ClinVar RCV Id: RCV000561357 RCV000698328 RCV001824831 RCV002264957 RCV002289777
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys390Arg
CA46710290
NM_001281493.2:c.1169A>G