Canonical Allele Identifier: PA2829429607
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile539Asn
CA309733
NM_003319.4:c.1616T>A