Canonical Allele Identifier: PA1139704551
Gene: FARSA HGNC NCBI

Linked Data

ClinVar Variation Id: 977639
ClinVar RCV Id: RCV001255421
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004452.1:p.Phe256Leu
CA305504171
NM_004461.3:c.766T>C
CA404284687
NM_004461.3:c.768C>G
CA404284688
NM_004461.3:c.768C>A