Canonical Allele Identifier: PA302552
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192075
ClinVar RCV Id: RCV000172467 RCV000642957 RCV000618905 RCV000765589 RCV000852932 RCV003150043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His2223Leu
CA302549
NM_001267550.2:c.6668A>T