Canonical Allele Identifier: PA2830196882
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290472
ClinVar RCV Id: RCV000259463 RCV000274681 RCV000317014 RCV000356634 RCV000366217 RCV000378536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala16835Pro
CA1992894
NM_133378.4:c.50503G>C