Canonical Allele Identifier: PA183249
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178895
ClinVar RCV Id: RCV000155667 RCV000643666 RCV000714077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gln22699His
CA183247
NM_001267550.2:c.68097G>C
CA349421653
NM_001267550.2:c.68097G>T