Canonical Allele Identifier: PA208676
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 212461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg4499Trp
CA208675
NM_133378.4:c.13495C>T