Canonical Allele Identifier: PA645412509
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238875
ClinVar RCV Id: RCV000232836 RCV000728833 RCV000764301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile33060Leu
CA1986243
NM_001267550.2:c.99178A>C
CA349430779
NM_001267550.2:c.99178A>T