Canonical Allele Identifier: PA916011491
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 660233
ClinVar RCV Id: RCV002325607 RCV000817387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly986Ser
CA346758747
NM_001281492.2:c.2956G>A