Canonical Allele Identifier: PA357901
Gene: ARHGEF10L HGNC NCBI

Linked Data

ClinVar Variation Id: 224809
ClinVar RCV Id: RCV000210382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060595.3:p.Asp1216Asn
CA357900
NM_018125.4:c.3646G>A