Canonical Allele Identifier: PA2830204299
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405037
ClinVar RCV Id: RCV000476896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly32598Val
CA16610295
NM_133378.4:c.97793G>T