Canonical Allele Identifier: PA2830193277
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238725
ClinVar RCV Id: RCV000234407 RCV000300616 RCV000491329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly7280Arg
CA2000194
NM_133378.4:c.21838G>A
CA349484119
NM_133378.4:c.21838G>C