Canonical Allele Identifier: PA2829433363
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn7105Ser
CA309923
NM_003319.4:c.21314A>G