Canonical Allele Identifier: PA181652
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178174
ClinVar RCV Id: RCV000154899 RCV000618633 RCV000769893 RCV000727232 RCV001079791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly29662Ser
CA181649
NM_001267550.2:c.88984G>A