Canonical Allele Identifier: PA2829437269
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96298
ClinVar RCV Id: RCV000082422 RCV000243614 RCV000209613 RCV000461211 RCV000765553 RCV000725504 RCV001131153 RCV001131152 RCV001131150 RCV001131151 RCV001134109 RCV003486642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu13877Lys
CA223957
NM_003319.4:c.41629G>A