Canonical Allele Identifier: PA2829446316
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser26774Arg
CA311295
NM_003319.4:c.80322T>G
CA349400210
NM_003319.4:c.80322T>A
CA349400215
NM_003319.4:c.80320A>C