Canonical Allele Identifier: PA2830221274
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47412
ClinVar RCV Id: RCV000040682 RCV000184884 RCV000620912 RCV000768904 RCV001086569 RCV001135731 RCV001135727 RCV001135728 RCV001135729 RCV001135730 RCV004534933
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly18557Arg
CA140926
NM_133432.3:c.55669G>A
CA349573256
NM_133432.3:c.55669G>C