Canonical Allele Identifier: PA2829431855
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser4265Phe
CA311752
NM_003319.4:c.12794C>T