Canonical Allele Identifier: CA993948946
Gene: CYP4F23P HGNC NCBI

Linked Data

dbSNP Id: rs1971716370

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15566847T>G , CM000681.2:g.15566847T>G GRCh38
NC_000019.9:g.15677658T>G , CM000681.1:g.15677658T>G GRCh37
NC_000019.8:g.15538658T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000593402.6:n.201+2573T>G