Canonical Allele Identifier: PA916066009
Gene: TTN HGNC NCBI
ClinVar RCV:
RCV000600741
ClinVar Variation:
509581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asp7388Asn
CA1994743
NM_133437.4:c.22162G>A