Canonical Allele Identifier: PA658808884
Gene: NIPA1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653200.2:p.Val135Met
CA7426096
NM_144599.5:c.403G>A