Canonical Allele Identifier: PA181760
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178200
ClinVar RCV Id: RCV000154931 RCV000319887 RCV000316262 RCV000293736 RCV000620398 RCV000374365 RCV000389492 RCV000725861 RCV001293206 RCV001081279 RCV004534973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro21845Leu
CA181757
NM_001267550.2:c.65534C>T