Canonical Allele Identifier: PA309153
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Thr2543Ser
CA309149
NM_133379.5:c.7628C>G
CA349679335
NM_133379.5:c.7627A>T