Canonical Allele Identifier: PA2826419135
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr18051Ala
CA1992720
NM_001256850.1:c.54151A>G