Canonical Allele Identifier: CA971893225
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152519_80152520del , CM000677.2:g.80152519_80152520del GRCh38
NC_000015.9:g.80444861_80444862del , CM000677.1:g.80444861_80444862del GRCh37
NC_000015.8:g.78231916_78231917del NCBI36
NG_012833.1:g.4521_4522del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-56_-55del ENSP00000453152.1:n.-56_-55del