Canonical Allele Identifier: CA2190326533

Gene: FAH

Linked Data

• dbSNP Id: rs2041054026

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152494dup , CM000677.2:g.80152494dup	GRCh38
NC_000015.9:g.80444836dup , CM000677.1:g.80444836dup	GRCh37
NC_000015.8:g.78231891dup	NCBI36
NG_012833.1:g.4496dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558022.5:c.-81dup	ENSP00000453152.1:n.-81dup