Canonical Allele Identifier: PA200063
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_001254479.2:p.Asn32797Asp
CA200061
NM_001267550.2:c.98389A>G