Canonical Allele Identifier: PA2830213131
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly4530Ser
CA179001
NM_133432.3:c.13588G>A