Canonical Allele Identifier: PA2830213024
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asp4329Glu
CA238155
NM_133432.3:c.12987T>G
CA349606837
NM_133432.3:c.12987T>A