Canonical Allele Identifier: PA2826423002
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_001243779.1:p.Glu25064Asp
CA346130
NM_001256850.1:c.75192G>T
CA349591216
NM_001256850.1:c.75192G>C