Canonical Allele Identifier: PA232532
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 137831
ClinVar RCV Id: RCV000126046 RCV000184059 RCV000617538 RCV000852924 RCV001081931 RCV001129535 RCV001129536 RCV001129537 RCV001129538 RCV001129539 RCV003149862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg3388Gln
CA232527
NM_133379.5:c.10163G>A