Canonical Allele Identifier: PA2829439467
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179544
ClinVar RCV Id: RCV000156336 RCV000206691 RCV000336649 RCV000389979 RCV000296905 RCV000303254 RCV000401815 RCV001311954 RCV001170791 RCV004544452 RCV002345518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu17640Asp
CA346130
NM_003319.4:c.52920G>T
CA349591216
NM_003319.4:c.52920G>C