Canonical Allele Identifier: PA2499240959
Gene: PEX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019602

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165558.2:p.Met191Leu
CA371557052
NM_001172087.2:c.571A>T
CA371557053
NM_001172087.2:c.571A>C