Canonical Allele Identifier: PA645410165
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283488
ClinVar RCV Id: RCV000337689 RCV000282260 RCV000302673 RCV000394206 RCV000318089 RCV000336131 RCV000619450 RCV000863478 RCV001798770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg17836His
CA1993799
NM_001267550.2:c.53507G>A