Canonical Allele Identifier: PA140118
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47143
ClinVar RCV Id: RCV000040413 RCV000642907 RCV002225278 RCV004541162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly19661Asp
CA140115
NM_001267550.2:c.58982G>A