Canonical Allele Identifier: PA2829434640
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser9387Pro
CA302469
NM_003319.4:c.28159T>C