Canonical Allele Identifier: PA2830195419
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile13271Thr
CA309893
NM_133378.4:c.39812T>C