Canonical Allele Identifier: PA2741965731
Gene: ARHGAP31 HGNC NCBI
ClinVar RCV:
RCV003579233
ClinVar Variation:
2703278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Lys39Arg
CA354349372
NM_020754.4:c.116A>G