Canonical Allele Identifier: PA237920
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile19081Thr
CA237918
NM_001267550.2:c.57242T>C