Canonical Allele Identifier: PA658664586
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466802
ClinVar RCV Id: RCV000554544 RCV000605220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr4227Ser
CA349610955
NM_001267550.2:c.12680C>G
CA349610964
NM_001267550.2:c.12679A>T