Canonical Allele Identifier: PA916028377
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 633068
ClinVar RCV Id: RCV000780930 RCV001277083 RCV003480813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr433Ser
CA388036144
NM_001330579.2:c.1298C>G
CA388036149
NM_001330579.2:c.1297A>T