Canonical Allele Identifier: PA2830207638
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263625
ClinVar RCV Id: RCV000248384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr8130Ala
CA10587508
NM_133378.4:c.24388A>G