Canonical Allele Identifier: PA2830219003
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile14711Ser
CA178526
NM_133432.3:c.44132T>G