Canonical Allele Identifier: PA2826626709
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3075039
ClinVar RCV Id: RCV004015565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp537Asn
CA346750661
NM_001281492.2:c.1609G>A