Canonical Allele Identifier: PA202128
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192152
ClinVar RCV Id: RCV000172632 RCV000176834 RCV000769938 RCV001086126 RCV001840213 RCV002336415 RCV001293185 RCV001840210 RCV001840211 RCV001840212 RCV004539590
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr26538Ala
CA202125
NM_001267550.2:c.79612A>G