Canonical Allele Identifier: PA2826417289
Gene: TTN HGNC NCBI
ClinVar RCV:
RCV000600741
ClinVar Variation:
509581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp14620Asn
CA1994743
NM_001256850.1:c.43858G>A