Canonical Allele Identifier: PA141532
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu30733Lys
CA141530
NM_133378.4:c.92197G>A