Canonical Allele Identifier: PA2826632384
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 433917
ClinVar RCV Id: RCV000502849 RCV002438211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu677Pro
CA346756212
NM_001281493.2:c.2030T>C