Canonical Allele Identifier: PA658816856
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn31962Asp
CA1986859
NM_001267550.2:c.95884A>G