Canonical Allele Identifier: PA2829442677
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala22628Asp
CA141318
NM_003319.4:c.67883C>A