Canonical Allele Identifier: PA658664844
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466869
ClinVar RCV Id: RCV000553414 RCV001547863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His6499Leu
CA2001385
NM_001267550.2:c.19496A>T