Canonical Allele Identifier: PA2829431663
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser3911Asn
CA238157
NM_003319.4:c.11732G>A