Canonical Allele Identifier: PA285792
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96327
ClinVar RCV Id: RCV000293378 RCV000259069 RCV000373025 RCV000294576 RCV000333239 RCV000385289 RCV000470580 RCV000723662 RCV002390246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val31905Ile
CA285790
NM_133378.4:c.95713G>A