Canonical Allele Identifier: PA178441
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165735
ClinVar RCV Id: RCV000152188 RCV000172199 RCV000309213 RCV000269133 RCV000367439 RCV000326590 RCV000402112 RCV000619946 RCV000642884 RCV001798477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg28327Gln
CA178440
NM_133378.4:c.84980G>A