Canonical Allele Identifier: PA2741850758
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2926013
ClinVar RCV Id: RCV003786299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Met687Leu
CA413598322
NM_001282224.2:c.2059A>C
CA413598324
NM_001282224.2:c.2059A>T