Canonical Allele Identifier: CA274010632

Gene: FAH

Linked Data

• dbSNP Id: rs34729999

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152518dup , CM000677.2:g.80152518dup	GRCh38
NC_000015.9:g.80444860dup , CM000677.1:g.80444860dup	GRCh37
NC_000015.8:g.78231915dup	NCBI36
NG_012833.1:g.4520dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558022.5:c.-57dup	ENSP00000453152.1:n.-57dup