Canonical Allele Identifier: PA181925
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile5619Val
CA181923
NM_001256850.1:c.16855A>G