Canonical Allele Identifier: CA971894184
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs1255857319

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152738A>G , CM000677.2:g.80152738A>G GRCh38
NC_000015.9:g.80445080A>G , CM000677.1:g.80445080A>G GRCh37
NC_000015.8:g.78232135A>G NCBI36
NG_012833.1:g.4740A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+193A>G ENSP00000453152.1:n.-30+193A>G