Canonical Allele Identifier: PA2829437897
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Lys14882Asn
CA289100
NM_003319.4:c.44646G>C
CA349650351
NM_003319.4:c.44646G>T