Canonical Allele Identifier: PA139890
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg14814Gly
CA139888
NM_133378.4:c.44440A>G