Canonical Allele Identifier: PA178442
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165735
ClinVar RCV Id: RCV000152188 RCV000172199 RCV000309213 RCV000269133 RCV000367439 RCV000326590 RCV000402112 RCV000619946 RCV000642884 RCV001798477
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg29254Gln
CA178440
NM_001256850.1:c.87761G>A