Canonical Allele Identifier: PA2829430100
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly1299Asp
CA283320
NM_003319.4:c.3896G>A