Canonical Allele Identifier: PA2830243238
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg26263Trp
CA1985267
NM_133437.4:c.78787C>T