Canonical Allele Identifier: PA2829437969
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191903
ClinVar RCV Id: RCV000172264 RCV000282942 RCV000288822 RCV000248880 RCV000259146 RCV000379211 RCV000347355 RCV000404979 RCV000769955 RCV000852813 RCV001084205 RCV002227932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Leu14984Pro
CA302449
NM_003319.4:c.44951T>C