Canonical Allele Identifier: PA916012578
Gene: ATP7A HGNC NCBI

Linked Data

ClinVar Variation Id: 640366
ClinVar RCV Id: RCV000793378 RCV002279531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269153.1:p.Met69Ile
CA10458895
NM_001282224.2:c.207G>A
CA413599027
NM_001282224.2:c.207G>T
CA413599029
NM_001282224.2:c.207G>C