Canonical Allele Identifier: PA103062
Gene: MTPAP HGNC NCBI

Linked Data

ClinVar Variation Id: 18391
ClinVar RCV Id: RCV000000002 RCV002513130
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060579.3:p.Asn478Asp
CA113782
NM_018109.3:c.1432A>G