Canonical Allele Identifier: PA2829433351
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229442
ClinVar RCV Id: RCV000214620 RCV002494575 RCV003327384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala7088Ser
CA10576523
NM_003319.4:c.21262G>T