Canonical Allele Identifier: PA140016
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47103
ClinVar RCV Id: RCV000040373 RCV000797680 RCV003156220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys18423Asn
CA140013
NM_001267550.2:c.55269G>C
CA349543218
NM_001267550.2:c.55269G>T