Canonical Allele Identifier: PA2829430368
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn1709Ser
CA238284
NM_003319.4:c.5126A>G