Canonical Allele Identifier: PA916066927
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser9579Pro
CA302469
NM_133437.4:c.28735T>C