Canonical Allele Identifier: PA178713
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165968
ClinVar RCV Id: RCV000152300 RCV000533354 RCV000727413 RCV000768986 RCV002433661
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr18460Ala
CA178711
NM_001267550.2:c.55378A>G