Canonical Allele Identifier: PA178831
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166024
ClinVar RCV Id: RCV000152345 RCV000343952 RCV000277761 RCV000291298 RCV000553961 RCV000330386 RCV000388479 RCV003137657 RCV002415642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr14352Asn
CA178829
NM_001256850.1:c.43055C>A