Canonical Allele Identifier: PA2826626403
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2682020
ClinVar RCV Id: RCV003477312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys468Asn
CA346749308
NM_001281492.2:c.1404A>T
CA346749310
NM_001281492.2:c.1404A>C