Canonical Allele Identifier: PA2830202824
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238875
ClinVar RCV Id: RCV000232836 RCV000728833 RCV000764301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile30492Leu
CA1986243
NM_133378.4:c.91474A>C
CA349430779
NM_133378.4:c.91474A>T