Canonical Allele Identifier: PA141264
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47524
ClinVar RCV Id: RCV000040793 RCV000226810 RCV001698952 RCV002362646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu30817Asp
CA141261
NM_001267550.2:c.92451G>T
CA349493240
NM_001267550.2:c.92451G>C