Canonical Allele Identifier: PA658814558
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 498614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn18193Ser
CA1993613
NM_001267550.2:c.54578A>G