Canonical Allele Identifier: PA2826425875
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467664
ClinVar RCV Id: RCV000560368 RCV000618293 RCV000993510 RCV001798890 RCV002252162 RCV003227786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala29862Thr
CA1987126
NM_001256850.1:c.89584G>A