Canonical Allele Identifier: PA200062
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192199
ClinVar RCV Id: RCV000172784
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn30229Asp
CA200061
NM_133378.4:c.90685A>G