Canonical Allele Identifier: CA971893272
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152536_80152537del , CM000677.2:g.80152536_80152537del GRCh38
NC_000015.9:g.80444878_80444879del , CM000677.1:g.80444878_80444879del GRCh37
NC_000015.8:g.78231933_78231934del NCBI36
NG_012833.1:g.4538_4539del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-39_-38del ENSP00000453152.1:n.-39_-38del