Canonical Allele Identifier: PA2829445410
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser25867Arg
CA311196
NM_003319.4:c.77601T>G
CA349410905
NM_003319.4:c.77601T>A
CA349410910
NM_003319.4:c.77599A>C