Canonical Allele Identifier: PA2830210677
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47018
ClinVar RCV Id: RCV000040288 RCV000225777 RCV000250117 RCV000288662 RCV000266423 RCV000323811 RCV000380733 RCV000385248 RCV000769135 RCV001530088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly1299Asp
CA283320
NM_133432.3:c.3896G>A