Canonical Allele Identifier: PA645410517
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn20870Thr
CA1992202
NM_001267550.2:c.62609A>C