Canonical Allele Identifier: PA2830223266
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282539
ClinVar RCV Id: RCV000334287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met21697Leu
CA10604211
NM_133432.3:c.65089A>T
CA349496003
NM_133432.3:c.65089A>C