Canonical Allele Identifier: PA310748
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu27453Lys
CA310747
NM_001256850.1:c.82357G>A