Canonical Allele Identifier: PA2829431251
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn3179Ser
CA141678
NM_003319.4:c.9536A>G