Canonical Allele Identifier: PA237880
Gene: TTN HGNC NCBI
ClinVar Allele:
189565
ClinVar RCV:
RCV000172286
ClinVar Variation:
191922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly18827Cys
CA237879
NM_133378.4:c.56479G>T