Canonical Allele Identifier: PA2830202655
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1757065
ClinVar RCV Id: RCV002365156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu30129Asp
CA1986445
NM_133378.4:c.90387A>C
CA349434898
NM_133378.4:c.90387A>T