Canonical Allele Identifier: PA915963887
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 818925
ClinVar RCV Id: RCV001011016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile442del
CA915943809
NM_000179.3:c.1324_1326del