Canonical Allele Identifier: PA2830194969
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp12094Glu
CA1995783
NM_133378.4:c.36282T>G
CA349646553
NM_133378.4:c.36282T>A