Canonical Allele Identifier: PA2829433062
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Leu6543Ser
CA139739
NM_003319.4:c.19628T>C