Canonical Allele Identifier: PA2830210778
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg1375Trp
CA181985
NM_133432.3:c.4123C>T