Canonical Allele Identifier: PA2830202167
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 132137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro29164Leu
CA358828
NM_133378.4:c.87491C>T