Canonical Allele Identifier: PA302716
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 193778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu8927Asp
CA302714
NM_133378.4:c.26781A>T
CA349569435
NM_133378.4:c.26781A>C