Canonical Allele Identifier: PA181562
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130690
ClinVar RCV Id: RCV000118803 RCV000154869 RCV000769847 RCV001086370 RCV002225083 RCV002390268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu31815Gln
CA181560
NM_133378.4:c.95443G>C