Canonical Allele Identifier: PA2573177247
Gene: ASL HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020117.1:p.Ile100Asn
CA4276894
NM_001024946.2:c.299T>A