Canonical Allele Identifier: PA645390227
Gene: ASNS HGNC NCBI

Linked Data

ClinVar Variation Id: 373307
ClinVar RCV Id: RCV000412830
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899199.2:p.Ser427Pro
CA16042617
NM_183356.4:c.1279T>C