Canonical Allele Identifier: PA2830213496
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 499001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Phe5204Ile
CA349654857
NM_133432.3:c.15610T>A