Canonical Allele Identifier: PA658680925
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483875
ClinVar RCV Id: RCV000562338 RCV001297529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr767Asn
CA346753028
NM_000179.3:c.2300C>A