Canonical Allele Identifier: PA2830204528
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2438042
ClinVar RCV Id: RCV003137207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser32917Phe
CA349405208
NM_133378.4:c.98750C>T