Canonical Allele Identifier: PA2825088117
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1770528
ClinVar RCV Id: RCV002387876 RCV003095012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val450Ile
CA46707941
NM_000179.3:c.1348G>A