Canonical Allele Identifier: PA2826625683
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455128
ClinVar RCV Id: RCV000538584 RCV000567668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys298Glu
CA067440
NM_001281492.2:c.892A>G