Canonical Allele Identifier: PA2830195630
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg13771Trp
CA1994704
NM_133378.4:c.41311C>T