Canonical Allele Identifier: CA2629872723
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152725del , CM000677.2:g.80152725del GRCh38
NC_000015.9:g.80445067del , CM000677.1:g.80445067del GRCh37
NC_000015.8:g.78232122del NCBI36
NG_012833.1:g.4727del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+180del ENSP00000453152.1:n.-30+180del