Canonical Allele Identifier: PA141008
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_001254479.2:p.Glu28232Asp
CA141005
NM_001267550.2:c.84696A>C
CA349558568
NM_001267550.2:c.84696A>T