Canonical Allele Identifier: PA2573193740
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1469597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser35352Pro
CA60953469
NM_001267550.2:c.106054T>C