Canonical Allele Identifier: PA2830229910
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr2497Ser
CA309149
NM_133437.4:c.7490C>G
CA349679335
NM_133437.4:c.7489A>T