Canonical Allele Identifier: PA2830239607
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1297569
ClinVar RCV Id: RCV001723337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn21773His
CA349495682
NM_133437.4:c.65317A>C