Canonical Allele Identifier: PA311200
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203087
ClinVar RCV Id: RCV000643178 RCV001704940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser33344Gly
CA311199
NM_001256850.1:c.100030A>G