Canonical Allele Identifier: PA2830197956
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202798
ClinVar RCV Id: RCV000643672 RCV001311238 RCV001798653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly19364Arg
CA310322
NM_133378.4:c.58090G>A
CA349432636
NM_133378.4:c.58090G>C