Canonical Allele Identifier: PA309013
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu10594Lys
CA309012
NM_001256850.1:c.31780G>A