Canonical Allele Identifier: PA2830221742
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47440
ClinVar RCV Id: RCV000040709 RCV000274794 RCV000332698 RCV000318173 RCV000387249 RCV000375092 RCV000726293 RCV001087454 RCV002345326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu19292Asp
CA141005
NM_133432.3:c.57876A>C
CA349558568
NM_133432.3:c.57876A>T