ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA127923
Gene: ALB
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000019862
ClinVar Variation:
18207
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000468.1:p.Glu594Lys
CA127922
NM_000477.7:c.1780G>A