Canonical Allele Identifier: PA238109
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192015
ClinVar RCV Id: RCV000172391 RCV000610152 RCV000642888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu5882Asp
CA238108
NM_133378.4:c.17646A>C
CA349535218
NM_133378.4:c.17646A>T