Canonical Allele Identifier: PA2826632049
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453198
ClinVar RCV Id: RCV003182653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu597Asp
CA346755312
NM_001281493.2:c.1791A>C
CA346755313
NM_001281493.2:c.1791A>T