Canonical Allele Identifier: PA237648
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191827
ClinVar RCV Id: RCV000172168 RCV000244016 RCV000578003 RCV000577929 RCV000578083 RCV000600352 RCV001078580 RCV004535169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg31093Lys
CA237647
NM_133378.4:c.93278G>A