Canonical Allele Identifier: PA141120
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47473
ClinVar RCV Id: RCV000040742 RCV000270510 RCV000327903 RCV000362829 RCV000384731 RCV000334082 RCV000618175 RCV000475243 RCV000725444 RCV001798192
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly26796Ser
CA141118
NM_133378.4:c.80386G>A