Canonical Allele Identifier: PA302471
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser16811Pro
CA302469
NM_001256850.1:c.50431T>C