Canonical Allele Identifier: PA141978
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47819
ClinVar RCV Id: RCV000041088 RCV000476484 RCV000727750 RCV002453334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala3823Thr
CA141976
NM_133432.3:c.11467G>A