Canonical Allele Identifier: PA178941
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166138
ClinVar RCV Id: RCV000152388 RCV000643023 RCV000769903 RCV001804863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg8121Trp
CA178940
NM_133378.4:c.24361C>T