Canonical Allele Identifier: PA2829430151
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser1354Thr
CA139816
NM_003319.4:c.4061G>C