Canonical Allele Identifier: PA2826631413
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587347
ClinVar RCV Id: RCV003350671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly450Cys
CA346752698
NM_001281493.2:c.1348G>T