Canonical Allele Identifier: PA2830207940
Gene: TTN HGNC NCBI
ClinVar RCV:
RCV000643674
ClinVar Variation:
535602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val30786Leu
CA349426853
NM_133378.4:c.92356G>C
CA349426854
NM_133378.4:c.92356G>T