Canonical Allele Identifier: PA311230
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203097
ClinVar RCV Id: RCV000185121 RCV000525111 RCV002408822 RCV003150076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr33520Asn
CA311229
NM_001256850.1:c.100559C>A