Canonical Allele Identifier: PA2829440458
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu19167Asp
CA141005
NM_003319.4:c.57501A>C
CA349558568
NM_003319.4:c.57501A>T