Canonical Allele Identifier: PA2830222308
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile20210Leu
CA1988318
NM_133432.3:c.60628A>T
CA349536393
NM_133432.3:c.60628A>C