Canonical Allele Identifier: PA2830243101
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr26120Met
CA311202
NM_133437.4:c.78359C>T