Canonical Allele Identifier: PA2826420059
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_001243779.1:p.Gly19754Cys
CA237879
NM_001256850.1:c.59260G>T