Canonical Allele Identifier: PA309152
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202343
ClinVar RCV Id: RCV000184185 RCV000643624 RCV000852929 RCV002390475
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr2543Ser
CA309149
NM_001267550.2:c.7628C>G
CA349679335
NM_001267550.2:c.7627A>T