Canonical Allele Identifier: PA1139675320
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 952383
ClinVar RCV Id: RCV001224487 RCV002447127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu818Ile
CA346754072
NM_000179.3:c.2452C>A