Canonical Allele Identifier: PA184589
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179523
ClinVar RCV Id: RCV000156313 RCV000184991 RCV000643636 RCV002372023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg29420His
CA184587
NM_001256850.1:c.88259G>A