Canonical Allele Identifier: PA2830195852
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202684

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu14322Ala
CA309974
NM_133378.4:c.42965A>C