Canonical Allele Identifier: PA2830193604
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1030139
ClinVar RCV Id: RCV001331624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro8134Ser
CA60964328
NM_133378.4:c.24400C>T