Canonical Allele Identifier: PA645379536
Gene: MMAA HGNC NCBI

Linked Data

ClinVar Variation Id: 347598
ClinVar RCV Id: RCV000673980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758454.1:p.Pro43Leu
CA10617102
NM_172250.3:c.128C>T