Canonical Allele Identifier: PA916066195
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 195639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val7820Ile
CA242127
NM_133437.4:c.23458G>A