Canonical Allele Identifier: PA181765
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178202
ClinVar RCV Id: RCV000154933 RCV000243930 RCV001086769 RCV001133876 RCV001133878 RCV000726451 RCV001133877 RCV001133879 RCV001133880 RCV001170815 RCV001293232 RCV001358656 RCV004544423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala18579Thr
CA181764
NM_133378.4:c.55735G>A