Canonical Allele Identifier: PA916011979
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483828
ClinVar Variation Id: 1732205
ClinVar RCV Id: RCV002459261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg870Ser
CA346760202
NM_001281494.2:c.2610A>T
CA346760203
NM_001281494.2:c.2610A>C