Canonical Allele Identifier: PA2830212851
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_597676.3:p.Thr3989Ser
CA349610955
NM_133432.3:c.11966C>G
CA349610964
NM_133432.3:c.11965A>T