Canonical Allele Identifier: PA237628
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191820
ClinVar RCV Id: RCV000172160 RCV001338738
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34276Gln
CA237626
NM_001267550.2:c.102827G>A