Canonical Allele Identifier: PA2829438382
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn15704Asp
CA310493
NM_003319.4:c.47110A>G