Canonical Allele Identifier: PA2829442299
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile22043Thr
CA1987318
NM_003319.4:c.66128T>C