Canonical Allele Identifier: PA2826419750
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn19229Thr
CA1992202
NM_001256850.1:c.57686A>C