Canonical Allele Identifier: PA2830212878
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser4036Asn
CA238157
NM_133432.3:c.12107G>A