Canonical Allele Identifier: PA181651
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_001243779.1:p.Gly28021Ser
CA181649
NM_001256850.1:c.84061G>A