Canonical Allele Identifier: PA2830193425
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238728
ClinVar RCV Id: RCV000230199 RCV000362897 RCV003150137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp7629Glu
CA1999959
NM_133378.4:c.22887C>A
CA349467085
NM_133378.4:c.22887C>G