Canonical Allele Identifier: PA302959
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196801
ClinVar RCV Id: RCV000177667 RCV000221018 RCV000620787 RCV000770121 RCV001080643 RCV001131079 RCV001134033 RCV001131080 RCV001131081 RCV001131082 RCV003227694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.His2508Arg
CA302955
NM_133378.4:c.7523A>G