Canonical Allele Identifier: PA916066553
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn8639Lys
CA223945
NM_133437.4:c.25917C>G
CA349573075
NM_133437.4:c.25917C>A