Canonical Allele Identifier: PA2830230749
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_597681.4:p.Thr4056Ser
CA349610955
NM_133437.4:c.12167C>G
CA349610964
NM_133437.4:c.12166A>T