Canonical Allele Identifier: PA2829431280
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser3225Ala
CA179212
NM_003319.4:c.9673T>G