Canonical Allele Identifier: PA645409760
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404688
ClinVar RCV Id: RCV000463928 RCV000604586 RCV000714032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp14280Glu
CA1996010
NM_001267550.2:c.42840T>G
CA349653714
NM_001267550.2:c.42840T>A