Canonical Allele Identifier: PA181754
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96296
ClinVar RCV Id: RCV000154930 RCV000272166 RCV000381758 RCV000329528 RCV000468946 RCV000289674 RCV000342201 RCV000619243 RCV000852823 RCV001798281 RCV001811388
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly19020Arg
CA181752
NM_133378.4:c.57058G>A
CA349436974
NM_133378.4:c.57058G>C