Canonical Allele Identifier: PA2826417286
Gene: TTN HGNC NCBI
ClinVar RCV:
RCV002275541
ClinVar Variation:
1701398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile14617Val
CA349608043
NM_001256850.1:c.43849A>G