Canonical Allele Identifier: PA179342
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166323
ClinVar RCV Id: RCV000152509 RCV000643675 RCV000770150 RCV000725635 RCV002345483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly1305Trp
CA179339
NM_133378.4:c.3913G>T