Canonical Allele Identifier: PA141658
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47667
ClinVar RCV Id: RCV000040936 RCV000082473 RCV000241855 RCV001084033 RCV000768829 RCV001135202 RCV001135203 RCV001135205 RCV001135204 RCV001135206 RCV004541196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala32183Pro
CA141656
NM_133378.4:c.96547G>C