Canonical Allele Identifier: PA311811
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203249
ClinVar RCV Id: RCV000279145 RCV000338828 RCV000323716 RCV000227527 RCV000373151 RCV000374753 RCV000592445 RCV000725625 RCV001170869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly5329Asp
CA311809
NM_001267550.2:c.15986G>A