Canonical Allele Identifier: PA2580449091
Gene: ALG9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079016.2:p.Pro451Arg
CA6274441
NM_024740.2:c.1352C>G