Canonical Allele Identifier: PA2829435742
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn11376Ser
CA140219
NM_003319.4:c.34127A>G