Canonical Allele Identifier: PA658680356
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483829
ClinVar RCV Id: RCV000568458 RCV001294425 RCV001574830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg298Gly
CA346740688
NM_000179.3:c.892C>G