Canonical Allele Identifier: PA2830231048
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly4597Ser
CA179001
NM_133437.4:c.13789G>A