Canonical Allele Identifier: PA309895
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile15839Thr
CA309893
NM_001267550.2:c.47516T>C