Canonical Allele Identifier: PA2830200120
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202905
ClinVar RCV Id: RCV000184873 RCV000619230 RCV000678759 RCV001086421 RCV001706158 RCV004537555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly24533Val
CA310647
NM_133378.4:c.73598G>T