Canonical Allele Identifier: PA184885
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179667
ClinVar RCV Id: RCV000156463 RCV000863688 RCV001507593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala19549Thr
CA184884
NM_133378.4:c.58645G>A