Canonical Allele Identifier: PA285786
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp30374Glu
CA285784
NM_133378.4:c.91122C>G
CA349431556
NM_133378.4:c.91122C>A