Canonical Allele Identifier: PA140222
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47172
ClinVar RCV Id: RCV000040442 RCV000118772 RCV000617338 RCV001086533 RCV004534915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn18800Ser
CA140219
NM_001256850.1:c.56399A>G