Canonical Allele Identifier: PA2826630305
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2161350
ClinVar RCV Id: RCV003078528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Cys194Gly
CA346746070
NM_001281493.2:c.580T>G