Canonical Allele Identifier: PA2826426039
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 132137
ClinVar RCV Id: RCV000119025 RCV002492403 RCV003987364 RCV003988827 RCV000684823 RCV000727672 RCV003343647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro30091Leu
CA358828
NM_001256850.1:c.90272C>T