Canonical Allele Identifier: PA2825631659
Gene: ACSF3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2134032
ClinVar RCV Id: RCV003044729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120686.1:p.Ser498Arg
CA8238236
NM_001127214.4:c.1494C>G
CA397148245
NM_001127214.4:c.1492A>C
CA397148251
NM_001127214.4:c.1494C>A