Canonical Allele Identifier: PA2826632328
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 857341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg663Gly
CA346756076
NM_001281493.2:c.1987A>G