Canonical Allele Identifier: PA302506
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn8626Ser
CA302503
NM_001267550.2:c.25877A>G