Canonical Allele Identifier: PA2829435644
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1730619
ClinVar RCV Id: RCV002321087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Pro11207Ser
CA60968658
NM_003319.4:c.33619C>T