Canonical Allele Identifier: PA138661
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46577
ClinVar RCV Id: RCV000039847 RCV000172723 RCV001081037 RCV001129649 RCV001129651 RCV001129648 RCV001129650 RCV001134674 RCV002381318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg3363His
CA138655
NM_133379.5:c.10088G>A