Canonical Allele Identifier: PA2826417328
Gene: TTN HGNC NCBI
ClinVar Allele:
449786
ClinVar RCV:
RCV000539933
ClinVar Variation:
467209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr14687Ile
CA1994713
NM_001256850.1:c.44060C>T