Canonical Allele Identifier: PA311260
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro1207Thr
CA311258
NM_001256850.1:c.3619C>A