Canonical Allele Identifier: PA2826497655
Gene: TTN HGNC NCBI
ClinVar RCV:
RCV002275541
ClinVar Variation:
1701398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile16258Val
CA349608043
NM_001267550.2:c.48772A>G