Canonical Allele Identifier: PA2830238832
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr20574Arg
CA181662
NM_133437.4:c.61721C>G