Canonical Allele Identifier: PA2573280286
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 1500701
ClinVar RCV Id: RCV002042632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065805.2:p.Pro779Ser
CA2554010
NM_020754.4:c.2335C>T