Canonical Allele Identifier: PA178478
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165799
ClinVar RCV Id: RCV000152203 RCV000332173 RCV000260100 RCV000370450 RCV000274661 RCV000366979 RCV000643482 RCV000768909 RCV001704096 RCV002345480 RCV004544366
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly27313Glu
CA178475
NM_001267550.2:c.81938G>A