Canonical Allele Identifier: PA658817382
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535017
ClinVar RCV Id: RCV000642773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile35460Thr
CA349405624
NM_001267550.2:c.106379T>C