Canonical Allele Identifier: PA658680542
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys428Glu
CA067440
NM_000179.3:c.1282A>G