Canonical Allele Identifier: PA2826627079
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu625Asp
CA346752788
NM_001281492.2:c.1875A>C
CA346752791
NM_001281492.2:c.1875A>T