Canonical Allele Identifier: PA2829436736
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191136
ClinVar RCV Id: RCV000171317 RCV000288338 RCV000303449 RCV000340260 RCV000343261 RCV000406446 RCV000544634 RCV001293233 RCV003137700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg13030Trp
CA236091
NM_003319.4:c.39088C>T