Canonical Allele Identifier: CA2190326621
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152520A= , CM000677.2:g.80152520A= GRCh38
NC_000015.9:g.80444862A= , CM000677.1:g.80444862A= GRCh37
NC_000015.8:g.78231917A= NCBI36
NG_012833.1:g.4522A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-55A= ENSP00000453152.1:n.-55A=