Canonical Allele Identifier: PA2829442965
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1755953
ClinVar RCV Id: RCV002362242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu22942Asp
CA1986838
NM_003319.4:c.68826A>C
CA349454817
NM_003319.4:c.68826A>T