Canonical Allele Identifier: PA2826424586
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile27730Thr
CA1988198
NM_001256850.1:c.83189T>C