Canonical Allele Identifier: PA310489
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202853
ClinVar RCV Id: RCV000184811 RCV000469626 RCV000734356 RCV001132750 RCV001131758 RCV001131759 RCV001131760 RCV001131761 RCV002336485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro24715Leu
CA310487
NM_001267550.2:c.74144C>T