Canonical Allele Identifier: PA2829436318
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asp12334Asn
CA310264
NM_003319.4:c.37000G>A