Canonical Allele Identifier: PA658815539
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535665
ClinVar RCV Id: RCV000643789 RCV000829330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr23769Ser
CA1990648
NM_001267550.2:c.71306C>G
CA1990651
NM_001267550.2:c.71305A>T