Canonical Allele Identifier: PA2825085434
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1947514
ClinVar RCV Id: RCV002685514 RCV004007539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro59Ala
CA346735004
NM_000179.3:c.175C>G