Canonical Allele Identifier: PA2829438482
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47332
ClinVar RCV Id: RCV000040602 RCV000249030 RCV000471721 RCV000768930 RCV001086359 RCV001128971 RCV001128973 RCV001128972 RCV001128974 RCV001131634 RCV004534927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gln15900His
CA140713
NM_003319.4:c.47700A>C
CA349630444
NM_003319.4:c.47700A>T