Canonical Allele Identifier: PA658817058
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535602
ClinVar RCV Id: RCV000643674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val33354Leu
CA349426853
NM_001267550.2:c.100060G>C
CA349426854
NM_001267550.2:c.100060G>T