Canonical Allele Identifier: PA179002
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166227
ClinVar RCV Id: RCV000152410 RCV000560224 RCV000725300 RCV002381481 RCV003486683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly3524Ser
CA179001
NM_133378.4:c.10570G>A