Canonical Allele Identifier: PA2830195568
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg13629Cys
CA1994784
NM_133378.4:c.40885C>T