Canonical Allele Identifier: PA2826421202
Gene: TTN HGNC NCBI
ClinVar Allele:
1319872
ClinVar RCV:
RCV001799228
ClinVar Variation:
1329185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn21752dup
CA2573051778
NM_001256850.1:c.65255_65257dup