Canonical Allele Identifier: CA971893129
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152508_80152513del , CM000677.2:g.80152508_80152513del GRCh38
NC_000015.9:g.80444850_80444855del , CM000677.1:g.80444850_80444855del GRCh37
NC_000015.8:g.78231905_78231910del NCBI36
NG_012833.1:g.4510_4515del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-67_-62del ENSP00000453152.1:n.-67_-62del