Canonical Allele Identifier: PA169279
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142738
ClinVar RCV Id: RCV000132112 RCV000168184 RCV000708894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile1283Val
CA014555
NM_000179.3:c.3847A>G