Canonical Allele Identifier: PA2826625160
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1467927
ClinVar RCV Id: RCV002370625 RCV001993529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr175Asn
CA346740726
NM_001281492.2:c.524C>A