Canonical Allele Identifier: PA140227
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile18829Thr
CA140224
NM_001256850.1:c.56486T>C