Canonical Allele Identifier: PA309747
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202610
ClinVar RCV Id: RCV000184496 RCV000229755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro11810His
CA309746
NM_001256850.1:c.35429C>A