Canonical Allele Identifier: PA238499
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val16702Leu
CA238498
NM_133378.4:c.50104G>C