Canonical Allele Identifier: PA2830209281
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2016721
ClinVar RCV Id: RCV002851719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr32773Ser
CA349407201
NM_133378.4:c.98318C>G
CA349407203
NM_133378.4:c.98317A>T