Canonical Allele Identifier: PA2741812019
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 2503908
ClinVar RCV Id: RCV003230899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Asn388Asp
CA3846948
NM_000255.4:c.1162A>G