Canonical Allele Identifier: PA2826426194
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr30267His
CA1986896
NM_001256850.1:c.90799T>C