Canonical Allele Identifier: CA2190326959
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs2041057321

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152633_80152644dup , CM000677.2:g.80152633_80152644dup GRCh38
NC_000015.9:g.80444975_80444986dup , CM000677.1:g.80444975_80444986dup GRCh37
NC_000015.8:g.78232030_78232041dup NCBI36
NG_012833.1:g.4635_4646dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+88_-30+99dup ENSP00000453152.1:n.-30+88_-30+99dup