Canonical Allele Identifier: PA2825089724
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791805
ClinVar RCV Id: RCV002450622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile825Leu
CA346754132
NM_000179.3:c.2473A>C