Canonical Allele Identifier: PA2499229335
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1013697
ClinVar RCV Id: RCV001312322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu755Lys
CA346752768
NM_000179.3:c.2263G>A