Canonical Allele Identifier: PA102808
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31134
ClinVar RCV Id: RCV000024130 RCV000185751 RCV003407360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120686.1:p.Arg558Trp
CA129703
NM_001127214.4:c.1672C>T