Canonical Allele Identifier: PA2826629531
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 449895
ClinVar RCV Id: RCV000520147 RCV002376964 RCV001066209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys9Glu
CA346740754
NM_001281493.2:c.25A>G