Canonical Allele Identifier: PA183248
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_596869.4:p.Gln20131His
CA183247
NM_133378.4:c.60393G>C
CA349421653
NM_133378.4:c.60393G>T