Canonical Allele Identifier: PA138645
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46573
ClinVar RCV Id: RCV000039843 RCV000464810 RCV000769835 RCV001509175 RCV002408527 RCV004534848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Cys34277Tyr
CA138642
NM_001256850.1:c.102830G>A