Canonical Allele Identifier: PA658659203
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466750
ClinVar RCV Id: RCV000547265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp35396Glu
CA349406705
NM_001267550.2:c.106188T>G
CA349406709
NM_001267550.2:c.106188T>A