Canonical Allele Identifier: PA185570
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_001243779.1:p.Ser22894Tyr
CA185568
NM_001256850.1:c.68681C>A