Canonical Allele Identifier: PA302542
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192064
ClinVar RCV Id: RCV000172453 RCV000412686 RCV000526576 RCV002381564 RCV002485115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Pro3236Leu
CA302537
NM_133379.5:c.9707C>T