Canonical Allele Identifier: PA2829445327
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser25790Tyr
CA10613205
NM_003319.4:c.77369C>A