Canonical Allele Identifier: PA2580507367
Gene: TTN HGNC NCBI
ClinVar RCV:
RCV002275541
ClinVar Variation:
1701398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile7385Val
CA349608043
NM_133437.4:c.22153A>G