Canonical Allele Identifier: PA311203
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr33352Met
CA311202
NM_001256850.1:c.100055C>T