Canonical Allele Identifier: PA916064980
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asp5407Gly
CA237989
NM_133437.4:c.16220A>G