Canonical Allele Identifier: PA2826635060
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser247Tyr
CA008999
NM_001281494.2:c.740C>A