Canonical Allele Identifier: PA916064502
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile539Asn
CA309733
NM_133437.4:c.1616T>A