Canonical Allele Identifier: PA141329
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47552
ClinVar RCV Id: RCV000040821 RCV000172617 RCV000620427 RCV001131620 RCV001079500 RCV001131619 RCV001131616 RCV001131617 RCV001131618 RCV001170761 RCV004534943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg29180Cys
CA141327
NM_133378.4:c.87538C>T