Canonical Allele Identifier: PA2826667934
Gene: PLXDC2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269665.1:p.Met428Leu
CA376249839
NM_001282736.2:c.1282A>C
CA376249840
NM_001282736.2:c.1282A>T