Canonical Allele Identifier: PA658813397
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497133
ClinVar RCV Id: RCV000595566 RCV000764341 RCV000643599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp8995Glu
CA1999892
NM_001267550.2:c.26985C>A
CA349459595
NM_001267550.2:c.26985C>G