Canonical Allele Identifier: PA916066421
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg8362Gln
CA310007
NM_133437.4:c.25085G>A