Canonical Allele Identifier: PA645384362
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428364
ClinVar RCV Id: RCV000491279 RCV001319687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1214Lys
CA346760621
NM_000179.3:c.3640G>A