Canonical Allele Identifier: PA2830224920
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser24047Phe
CA311070
NM_133432.3:c.72140C>T