Canonical Allele Identifier: PA181842
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178227
ClinVar RCV Id: RCV000154962 RCV000206371 RCV000244036 RCV001135639 RCV001135637 RCV001135638 RCV001134139 RCV001134140 RCV001531333 RCV004544427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val10548Leu
CA181841
NM_001256850.1:c.31642G>C