Canonical Allele Identifier: PA645499372
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 282998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000043.4:p.Thr574Arg
CA10459092
NM_000052.7:c.1721C>G