Canonical Allele Identifier: PA2826627790
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455218
ClinVar RCV Id: RCV000549264 RCV002438283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu789Lys
CA346755427
NM_001281492.2:c.2365G>A