Canonical Allele Identifier: PA2826419432
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1730619
ClinVar RCV Id: RCV002321087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro18631Ser
CA60968658
NM_001256850.1:c.55891C>T