Canonical Allele Identifier: PA185571
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179981
ClinVar RCV Id: RCV000156784 RCV000172640 RCV000284991 RCV000315675 RCV000373849 RCV000340019 RCV000415309 RCV000379391 RCV000643266 RCV002336337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser24535Tyr
CA185568
NM_001267550.2:c.73604C>A