Canonical Allele Identifier: PA913192075
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 629847
ClinVar RCV Id: RCV000774590 RCV001856091 RCV002285413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu221Lys
CA073319
NM_000179.3:c.661G>A