Canonical Allele Identifier: PA916066425
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro8365Ser
CA1994134
NM_133437.4:c.25093C>T