Canonical Allele Identifier: PA2826624446
Gene: MLPH HGNC NCBI

Linked Data

ClinVar Variation Id: 4268
ClinVar RCV Id: RCV000004489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268403.1:p.Arg35Trp
CA116747
NM_001281474.2:c.103C>T