Canonical Allele Identifier: PA2829439939
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191880
ClinVar RCV Id: RCV000172237 RCV000259150 RCV000294267 RCV000335482 RCV000296920 RCV000351562 RCV000386155 RCV001085422 RCV002345592 RCV003150040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr18347Lys
CA302434
NM_003319.4:c.55040C>A