Canonical Allele Identifier: PA2830209130
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr32425Met
CA311202
NM_133378.4:c.97274C>T