Canonical Allele Identifier: PA2826630031
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys126Glu
CA067440
NM_001281493.2:c.376A>G