Canonical Allele Identifier: PA2826489614
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332937
ClinVar RCV Id: RCV000269589 RCV000282834 RCV000321505 RCV000327007 RCV000371165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp3397Glu
CA2004154
NM_001267550.2:c.10191C>A
CA349673502
NM_001267550.2:c.10191C>G