Canonical Allele Identifier: PA916066364
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val8210Phe
CA310001
NM_133437.4:c.24628G>T