Canonical Allele Identifier: PA2830204492
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3027063
ClinVar RCV Id: RCV003887456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly32857Arg
CA1985138
NM_133378.4:c.98569G>C
CA349406365
NM_133378.4:c.98569G>A