Canonical Allele Identifier: PA238288
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192083
ClinVar RCV Id: RCV000172475 RCV000259138 RCV000476288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Asn1755Ser
CA238284
NM_133379.5:c.5264A>G