Canonical Allele Identifier: CA971894163
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs1203622130

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152727A>T , CM000677.2:g.80152727A>T GRCh38
NC_000015.9:g.80445069A>T , CM000677.1:g.80445069A>T GRCh37
NC_000015.8:g.78232124A>T NCBI36
NG_012833.1:g.4729A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+182A>T ENSP00000453152.1:n.-30+182A>T