Canonical Allele Identifier: PA2580177339
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1906541
ClinVar RCV Id: RCV002586988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys35393Asn
CA349406755
NM_001267550.2:c.106179G>T
CA349406757
NM_001267550.2:c.106179G>C