Canonical Allele Identifier: CA971893195
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs2041054653

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152518_80152522del , CM000677.2:g.80152518_80152522del GRCh38
NC_000015.9:g.80444860_80444864del , CM000677.1:g.80444860_80444864del GRCh37
NC_000015.8:g.78231915_78231919del NCBI36
NG_012833.1:g.4520_4524del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-57_-53del ENSP00000453152.1:n.-57_-53del