Canonical Allele Identifier: PA1139675060
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 897269
ClinVar RCV Id: RCV001362434 RCV002445397 RCV001140445 RCV003462638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr786His
CA068860
NM_000179.3:c.2356T>C