Canonical Allele Identifier: PA2826632829
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 439207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu779Trp
CA346758098
NM_001281493.2:c.2336T>G