Canonical Allele Identifier: CA2559598051
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152674A>T , CM000677.2:g.80152674A>T GRCh38
NC_000015.9:g.80445016A>T , CM000677.1:g.80445016A>T GRCh37
NC_000015.8:g.78232071A>T NCBI36
NG_012833.1:g.4676A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+129A>T ENSP00000453152.1:n.-30+129A>T