Canonical Allele Identifier: PA2829432142
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val4765Ile
CA309778
NM_003319.4:c.14293G>A