Canonical Allele Identifier: PA181687
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178183
ClinVar RCV Id: RCV000154910 RCV000172226 RCV000225816 RCV000348240 RCV000295690 RCV000299304 RCV000404249 RCV000356815 RCV002345503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile26409Val
CA181685
NM_001256850.1:c.79225A>G