Canonical Allele Identifier: PA309559
Gene: TTN HGNC NCBI
ClinVar Allele:
199456
ClinVar RCV:
RCV000184421
ClinVar Variation:
202549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn9728Ser
CA309557
NM_001267550.2:c.29183A>G