Canonical Allele Identifier: PA2826636416
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2736254
ClinVar RCV Id: RCV003593392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu561Lys
CA346754825
NM_001281494.2:c.1681G>A