Canonical Allele Identifier: PA2830224277
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr23107Met
CA141358
NM_133432.3:c.69320C>T