Canonical Allele Identifier: PA2825631660
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2233742
ClinVar RCV Id: RCV002718090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120686.1:p.Ile499Val
CA397148253
NM_001127214.4:c.1495A>G