Canonical Allele Identifier: PA658680413
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser330Pro
CA073692
NM_000179.3:c.988T>C