Canonical Allele Identifier: CA783662220
Gene: CYP4F23P HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15566899G>C , CM000681.2:g.15566899G>C GRCh38
NC_000019.9:g.15677710G>C , CM000681.1:g.15677710G>C GRCh37
NC_000019.8:g.15538710G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000593402.6:n.201+2625G>C
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