Canonical Allele Identifier: PA182009
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178275
ClinVar RCV Id: RCV000155016 RCV000172492 RCV000266151 RCV000300150 RCV000305734 RCV000345372 RCV000358208 RCV000643424 RCV002399548
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala529Thr
CA182006
NM_133378.4:c.1585G>A