Canonical Allele Identifier: PA2829437305
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala13950Val
CA1990999
NM_003319.4:c.41849C>T