Canonical Allele Identifier: PA2829445962
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1004601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly26398Arg
CA349405587
NM_003319.4:c.79192G>A
CA349405590
NM_003319.4:c.79192G>C