Canonical Allele Identifier: PA916061285
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467028
ClinVar RCV Id: RCV000544688 RCV001130792 RCV001130794 RCV001130796 RCV001130793 RCV001130795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala9867Thr
CA1998386
NM_133378.4:c.29599G>A