Canonical Allele Identifier: PA658816593
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 499307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu29920Asp
CA1987872
NM_001267550.2:c.89760A>C
CA349516193
NM_001267550.2:c.89760A>T