Canonical Allele Identifier: PA2580485857
Gene: PLXDC2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116201.7:p.Met477Leu
CA376249839
NM_032812.9:c.1429A>C
CA376249840
NM_032812.9:c.1429A>T