Canonical Allele Identifier: PA2830236248
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro16355Ser
CA310517
NM_133437.4:c.49063C>T