Canonical Allele Identifier: PA2826632336
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1447968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr664Ala
CA346756089
NM_001281493.2:c.1990A>G