Canonical Allele Identifier: CA2629872455
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152533C>A , CM000677.2:g.80152533C>A GRCh38
NC_000015.9:g.80444875C>A , CM000677.1:g.80444875C>A GRCh37
NC_000015.8:g.78231930C>A NCBI36
NG_012833.1:g.4535C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-42C>A ENSP00000453152.1:n.-42C>A