Canonical Allele Identifier: PA2829430021
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly1157Ala
CA2005517
NM_003319.4:c.3470G>C