Canonical Allele Identifier: PA285782
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96303
ClinVar RCV Id: RCV001082586 RCV000617309 RCV000725164 RCV003486643 RCV002265602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr23225Ala
CA285779
NM_001256850.1:c.69673A>G