Canonical Allele Identifier: PA2826491940
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535063
ClinVar RCV Id: RCV000642830 RCV002440296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Phe989Leu
CA2005674
NM_001267550.2:c.2967C>A
CA349491103
NM_001267550.2:c.2967C>G
CA349491153
NM_001267550.2:c.2965T>C