Canonical Allele Identifier: PA302517
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr4640Pro
CA302515
NM_001256850.1:c.13918A>C