Canonical Allele Identifier: PA645502949
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 377432
ClinVar RCV Id: RCV000444454 RCV001245382 RCV002282137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777577.2:p.Glu490Asp
CA8238230
NM_174917.5:c.1470G>C
CA397148203
NM_174917.5:c.1470G>T