Canonical Allele Identifier: PA141334
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47555
ClinVar RCV Id: RCV000040824 RCV000082453 RCV000620998 RCV000852787 RCV001082921 RCV001134487 RCV001798200 RCV001135944 RCV001135945 RCV001135946 RCV001135947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser29198Phe
CA141332
NM_133378.4:c.87593C>T