Canonical Allele Identifier: PA2830219181
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Lys15007Asn
CA289100
NM_133432.3:c.45021G>C
CA349650351
NM_133432.3:c.45021G>T