Canonical Allele Identifier: PA2830204427
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn32780Lys
CA1985172
NM_133378.4:c.98340C>A
CA349407154
NM_133378.4:c.98340C>G