Canonical Allele Identifier: PA2499243614
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1004601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly35463Arg
CA349405587
NM_001267550.2:c.106387G>A
CA349405590
NM_001267550.2:c.106387G>C