Canonical Allele Identifier: CA971893251
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152523_80152525del , CM000677.2:g.80152523_80152525del GRCh38
NC_000015.9:g.80444865_80444867del , CM000677.1:g.80444865_80444867del GRCh37
NC_000015.8:g.78231920_78231922del NCBI36
NG_012833.1:g.4525_4527del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-52_-50del ENSP00000453152.1:n.-52_-50del