Canonical Allele Identifier: PA2830202971
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile30785Thr
CA1986083
NM_133378.4:c.92354T>C