Canonical Allele Identifier: PA140198
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47166
ClinVar RCV Id: RCV000040436 RCV000545067 RCV001128998 RCV001128997 RCV001135973 RCV001135975 RCV001135974 RCV001719774 RCV003335072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser1772Gly
CA140193
NM_133378.4:c.5314A>G