Canonical Allele Identifier: PA916066838
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229464
ClinVar RCV Id: RCV000216545 RCV000471303 RCV000852841 RCV002433936 RCV003137813 RCV004532766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro9300Ser
CA1993619
NM_133437.4:c.27898C>T