Canonical Allele Identifier: PA302529
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192062
ClinVar RCV Id: RCV000172451 RCV000462612 RCV001563648 RCV002466253 RCV002500451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Glu3419Asp
CA302528
NM_133437.4:c.10257G>C
CA349670461
NM_133437.4:c.10257G>T