Allele Registry

Canonical Allele Identifier: PA102857

Gene: ACSF3 HGNC NCBI

ClinVar RCV:

RCV000024136

RCV003114202

ClinVar Variation:

31140

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120686.1:p.Pro243Leu	CA129715 NM_001127214.4:c.728C>T