Canonical Allele Identifier: PA138874
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46653
ClinVar RCV Id: RCV000039923 RCV000154091 RCV000769064 RCV001134665 RCV001134666 RCV001134662 RCV001134664 RCV001086633 RCV001134663 RCV004534862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro5140Thr
CA138872
NM_133378.4:c.15418C>A