Canonical Allele Identifier: CA2629872476
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152562A>T , CM000677.2:g.80152562A>T GRCh38
NC_000015.9:g.80444904A>T , CM000677.1:g.80444904A>T GRCh37
NC_000015.8:g.78231959A>T NCBI36
NG_012833.1:g.4564A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+17A>T ENSP00000453152.1:n.-30+17A>T