Canonical Allele Identifier: CA971893851
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152661dup , CM000677.2:g.80152661dup GRCh38
NC_000015.9:g.80445003dup , CM000677.1:g.80445003dup GRCh37
NC_000015.8:g.78232058dup NCBI36
NG_012833.1:g.4663dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+116dup ENSP00000453152.1:n.-30+116dup