Canonical Allele Identifier: PA2826635999
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Cys463Ser
CA346752969
NM_001281494.2:c.1387T>A
CA346752975
NM_001281494.2:c.1388G>C