Canonical Allele Identifier: PA2829439725
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Pro18008Ser
CA1989238
NM_003319.4:c.54022C>T