Canonical Allele Identifier: PA346132
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_001254479.2:p.Glu26705Asp
CA346130
NM_001267550.2:c.80115G>T
CA349591216
NM_001267550.2:c.80115G>C