Canonical Allele Identifier: PA916066124
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Trp7598Cys
CA139810
NM_133437.4:c.22794G>T
CA349604648
NM_133437.4:c.22794G>C