Canonical Allele Identifier: CA971893668
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs2041057419

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152635_80152639dup , CM000677.2:g.80152635_80152639dup GRCh38
NC_000015.9:g.80444977_80444981dup , CM000677.1:g.80444977_80444981dup GRCh37
NC_000015.8:g.78232032_78232036dup NCBI36
NG_012833.1:g.4637_4641dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+90_-30+94dup ENSP00000453152.1:n.-30+90_-30+94dup