Canonical Allele Identifier: PA2825091779
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1006973
ClinVar RCV Id: RCV001304095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met1184_Ser1185delinsIle
CA2496052963
NM_000179.3:c.3552_3554del