Canonical Allele Identifier: PA2826629187
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 619879
ClinVar RCV Id: RCV000759872 RCV001036809 RCV002256494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn1177Tyr
CA346761456
NM_001281492.2:c.3529A>T