Canonical Allele Identifier: PA645468677
Gene: FIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 254671
ClinVar RCV Id: RCV000416491 RCV000688613 RCV001508193 RCV001095518 RCV001172960 RCV001154064 RCV003165682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055660.1:p.Tyr647Cys
CA3956233
NM_014845.6:c.1940A>G