Canonical Allele Identifier: PA2827326105
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3075464
ClinVar RCV Id: RCV004016982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Thr816Ser
CA388034332
NM_001330578.2:c.2447C>G
CA388034335
NM_001330578.2:c.2446A>T