Canonical Allele Identifier: PA2830209300
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Tyr27832Phe
CA310866
NM_133378.4:c.83495A>T