Canonical Allele Identifier: PA2830215033
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val7985Ala
CA309980
NM_133432.3:c.23954T>C