Canonical Allele Identifier: PA181742
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178196
ClinVar RCV Id: RCV000154926 RCV000172272 RCV000248442 RCV000234385 RCV000262197 RCV000370118 RCV000261085 RCV000316255 RCV000375502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu20245Lys
CA181741
NM_133378.4:c.60733G>A