Canonical Allele Identifier: PA2830195554
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn13602Ser
CA309923
NM_133378.4:c.40805A>G