Canonical Allele Identifier: PA302421
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191858
ClinVar RCV Id: RCV000172206 RCV000317539 RCV001130534 RCV001130536 RCV000852797 RCV001083916 RCV001130533 RCV001130535 RCV001130537 RCV002362885 RCV004539584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr29903Ser
CA302419
NM_001267550.2:c.89708C>G
CA349516699
NM_001267550.2:c.89707A>T