Canonical Allele Identifier: PA311738
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203226
ClinVar RCV Id: RCV000643391 RCV000729230
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn3818Ser
CA311737
NM_001256850.1:c.11453A>G