Canonical Allele Identifier: PA2826631496
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2502856
ClinVar RCV Id: RCV003229514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly468Cys
CA346753105
NM_001281493.2:c.1402G>T