Canonical Allele Identifier: PA184935
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179686
ClinVar RCV Id: RCV000156482 RCV000459869 RCV000764308 RCV002345519 RCV003137682 RCV004535010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn25565Ser
CA184934
NM_133378.4:c.76694A>G