Canonical Allele Identifier: PA2829443431
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47593
ClinVar RCV Id: RCV000040862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Leu23634Phe
CA141461
NM_003319.4:c.70900C>T