Canonical Allele Identifier: PA2830193472
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497133
ClinVar RCV Id: RCV000595566 RCV000764341 RCV000643599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp7751Glu
CA1999892
NM_133378.4:c.23253C>A
CA349459595
NM_133378.4:c.23253C>G