Canonical Allele Identifier: PA181585
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg32120Trp
CA181583
NM_001256850.1:c.96358C>T