Canonical Allele Identifier: CA971893146
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152512_80152518del , CM000677.2:g.80152512_80152518del GRCh38
NC_000015.9:g.80444854_80444860del , CM000677.1:g.80444854_80444860del GRCh37
NC_000015.8:g.78231909_78231915del NCBI36
NG_012833.1:g.4514_4520del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-63_-57del ENSP00000453152.1:n.-63_-57del