Canonical Allele Identifier: CA2190326889
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs1595888269

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152608T>G , CM000677.2:g.80152608T>G GRCh38
NC_000015.9:g.80444950T>G , CM000677.1:g.80444950T>G GRCh37
NC_000015.8:g.78232005T>G NCBI36
NG_012833.1:g.4610T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+63T>G ENSP00000453152.1:n.-30+63T>G