Canonical Allele Identifier: PA2830192775
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203300
ClinVar RCV Id: RCV000213535 RCV000251604 RCV000296518 RCV000335093 RCV000338709 RCV000401816 RCV000406874 RCV000470210 RCV000725490 RCV000770079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser5975Phe
CA311968
NM_133378.4:c.17924C>T