Canonical Allele Identifier: CA971893489
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152583del , CM000677.2:g.80152583del GRCh38
NC_000015.9:g.80444925del , CM000677.1:g.80444925del GRCh37
NC_000015.8:g.78231980del NCBI36
NG_012833.1:g.4585del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+38del ENSP00000453152.1:n.-30+38del