Canonical Allele Identifier: PA141957
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47811
ClinVar RCV Id: RCV000041080 RCV000725031 RCV001171051 RCV001081319 RCV002399394 RCV004537137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr3891Ile
CA141953
NM_001267550.2:c.11672C>T