Canonical Allele Identifier: PA2829435203
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser10402Thr
CA60971692
NM_003319.4:c.31204T>A