Canonical Allele Identifier: PA658809822
Gene: FIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 543496
ClinVar RCV Id: RCV000654270 RCV001154805 RCV001154806 RCV002360664 RCV003488768 RCV003918092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055660.1:p.Gly214Arg
CA3955852
NM_014845.6:c.640G>A
CA365219737
NM_014845.6:c.640G>C