Canonical Allele Identifier: PA2829432292
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 499001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Phe5079Ile
CA349654857
NM_003319.4:c.15235T>A