Canonical Allele Identifier: PA2830192402
Gene: TTN HGNC NCBI
ClinVar RCV:
RCV000642841
ClinVar Variation:
535073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala4943Val
CA2001600
NM_133378.4:c.14828C>T