Canonical Allele Identifier: PA2830224782
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192199
ClinVar RCV Id: RCV000172784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn23857Asp
CA200061
NM_133432.3:c.71569A>G