Canonical Allele Identifier: PA2826586968
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1514164
ClinVar RCV Id: RCV002026541 RCV003303649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile1011Phe
CA346761495
NM_001281494.2:c.3031A>T