Canonical Allele Identifier: PA2829441830
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Tyr21335Phe
CA310866
NM_003319.4:c.64004A>T