Canonical Allele Identifier: PA138673
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46585
ClinVar RCV Id: RCV000039855 RCV000185316 RCV000554346 RCV000769089 RCV000619842 RCV001132041 RCV001132979 RCV001132980 RCV001132981 RCV001132982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp4427Glu
CA138670
NM_001256850.1:c.13281C>A
CA349602499
NM_001256850.1:c.13281C>G