Canonical Allele Identifier: CA2190326596
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152512A= , CM000677.2:g.80152512A= GRCh38
NC_000015.9:g.80444854A= , CM000677.1:g.80444854A= GRCh37
NC_000015.8:g.78231909A= NCBI36
NG_012833.1:g.4514A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-63A= ENSP00000453152.1:n.-63A=