Canonical Allele Identifier: PA141326
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47549
ClinVar RCV Id: RCV000040818 RCV000765538 RCV000726197
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly31695Arg
CA141322
NM_001267550.2:c.95083G>A
CA349466615
NM_001267550.2:c.95083G>C