Canonical Allele Identifier: PA311489
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203155
ClinVar RCV Id: RCV000538379 RCV002390484 RCV001704945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ile2586Met
CA311485
NM_133379.5:c.7758A>G