Canonical Allele Identifier: PA310498
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202856
ClinVar RCV Id: RCV000184814 RCV001136046 RCV001136047 RCV001129081 RCV002336487 RCV001129080 RCV001136048 RCV003137736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr24855Ile
CA310496
NM_001267550.2:c.74564C>T