Canonical Allele Identifier: PA110042
Gene: TPM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003280.2:p.Arg133Pro
CA232647
NM_003289.4:c.398G>C