Canonical Allele Identifier: PA141381
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47569
ClinVar RCV Id: RCV000040838 RCV000643268 RCV000767014 RCV004018903 RCV002504916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala32096Thr
CA141378
NM_001267550.2:c.96286G>A