Canonical Allele Identifier: PA2825089048
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567467
ClinVar RCV Id: RCV003278517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro656His
CA346750595
NM_000179.3:c.1967C>A