Canonical Allele Identifier: PA2826428981
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2021348
ClinVar RCV Id: RCV002862585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu33708Pro
CA349407149
NM_001256850.1:c.101123T>C