Canonical Allele Identifier: PA139332
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46841
ClinVar RCV Id: RCV000040111 RCV000172682 RCV000577956 RCV000578036 RCV000578117 RCV001129423 RCV000852879 RCV001084360 RCV001129424 RCV004541143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val8996Phe
CA139329
NM_133378.4:c.26986G>T