Canonical Allele Identifier: PA2826632837
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719941
ClinVar RCV Id: RCV002304092 RCV002325726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu781Lys
CA346758114
NM_001281493.2:c.2341G>A