Canonical Allele Identifier: PA2830195600
Gene: TTN HGNC NCBI
ClinVar RCV:
RCV000600741
ClinVar Variation:
509581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp13693Asn
CA1994743
NM_133378.4:c.41077G>A