Canonical Allele Identifier: PA2826630829
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 224580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser314Cys
CA068191
NM_001281493.2:c.941C>G