Canonical Allele Identifier: PA2826629679
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser44Cys
CA16610875
NM_001281493.2:c.131C>G