Canonical Allele Identifier: PA2826413020
Gene: TTN HGNC NCBI
ClinVar RCV:
RCV000642841
ClinVar Variation:
535073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala5870Val
CA2001600
NM_001256850.1:c.17609C>T