Canonical Allele Identifier: PA2830202334
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1755953
ClinVar RCV Id: RCV002362242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu29439Asp
CA1986838
NM_133378.4:c.88317A>C
CA349454817
NM_133378.4:c.88317A>T