Canonical Allele Identifier: PA645412833
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile35218Thr
CA1985224
NM_001267550.2:c.105653T>C