Canonical Allele Identifier: PA2830195586
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro13675Thr
CA1994759
NM_133378.4:c.41023C>A