Canonical Allele Identifier: PA095882
Gene: FIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721
ClinVar RCV Id: RCV000001791 RCV000143812 RCV000416487 RCV000476702 RCV001270162 RCV001095515 RCV001330564 RCV001535566 RCV002362551 RCV003952336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055660.1:p.Ile41Thr
CA233088
NM_014845.6:c.122T>C