Canonical Allele Identifier: PA310721
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202929
ClinVar RCV Id: RCV000184906 RCV000461663 RCV002354506 RCV002298512 RCV002500561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly28372Glu
CA310719
NM_001267550.2:c.85115G>A