Canonical Allele Identifier: PA2829431587
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn3772Ser
CA311737
NM_003319.4:c.11315A>G