Canonical Allele Identifier: PA310495
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn24769Asp
CA310493
NM_001267550.2:c.74305A>G