Canonical Allele Identifier: PA302589
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192099
ClinVar RCV Id: RCV000172495 RCV000524658 RCV000577960 RCV000578069 RCV000578038 RCV001142583 RCV001142582 RCV001281537 RCV002433758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala89Gly
CA302585
NM_133378.4:c.266C>G