Canonical Allele Identifier: PA2826412086
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser3957Asn
CA238157
NM_001256850.1:c.11870G>A