Canonical Allele Identifier: PA309089
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202324
ClinVar RCV Id: RCV000184164 RCV000727333 RCV001088146 RCV002326998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala21433Thr
CA309088
NM_133378.4:c.64297G>A