Canonical Allele Identifier: PA302392
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191829
ClinVar RCV Id: RCV000172170 RCV000311753 RCV000315180 RCV000362844 RCV000270805 RCV000403284 RCV000517499 RCV001087486 RCV002381562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Cys30841Tyr
CA302391
NM_133378.4:c.92522G>A