Canonical Allele Identifier: PA645499377
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 388532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000043.4:p.Thr601Asn
CA10459112
NM_000052.7:c.1802C>A