Canonical Allele Identifier: PA2826628918
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 824176
ClinVar RCV Id: RCV001021079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp1125Asn
CA346761109
NM_001281492.2:c.3373G>A