Canonical Allele Identifier: PA2829437276
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly13890Ala
CA181737
NM_003319.4:c.41669G>C