Canonical Allele Identifier: PA645468629
Gene: FIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 407082
ClinVar RCV Id: RCV000462434 RCV000662128 RCV000662129 RCV000662127 RCV001573278 RCV000662126 RCV002411445 RCV001662424 RCV003970280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055660.1:p.Lys278Asn
CA3955919
NM_014845.6:c.834A>T
CA365220909
NM_014845.6:c.834A>C