Canonical Allele Identifier: CA2629872519
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152606del , CM000677.2:g.80152606del GRCh38
NC_000015.9:g.80444948del , CM000677.1:g.80444948del GRCh37
NC_000015.8:g.78232003del NCBI36
NG_012833.1:g.4608del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+61del ENSP00000453152.1:n.-30+61del