Canonical Allele Identifier: PA2826631977
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys583Asn
CA346755177
NM_001281493.2:c.1749A>C
CA346755178
NM_001281493.2:c.1749A>T