Canonical Allele Identifier: PA310411
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202827
ClinVar RCV Id: RCV000643517 RCV000764321 RCV001721160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr23524Ala
CA310409
NM_001267550.2:c.70570A>G