Canonical Allele Identifier: PA138855
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46646
ClinVar RCV Id: RCV000039916 RCV000082364 RCV000262868 RCV000302779 RCV000296922 RCV000355321 RCV000342596 RCV001082917 RCV000852901 RCV001798131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn5958Ser
CA138852
NM_001256850.1:c.17873A>G