Canonical Allele Identifier: PA310053
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu16286Pro
CA310052
NM_001256850.1:c.48857T>C