Canonical Allele Identifier: CA2629872710
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152725_80152773del , CM000677.2:g.80152725_80152773del GRCh38
NC_000015.9:g.80445067_80445115del , CM000677.1:g.80445067_80445115del GRCh37
NC_000015.8:g.78232122_78232170del NCBI36
NG_012833.1:g.4727_4775del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+180_-30+228del ENSP00000453152.1:n.-30+180_-30+228del