ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA123565
Gene: ERBB2
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.3319747859
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000014887
RCV000120744
RCV001511302
ClinVar Variation:
13873
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_004439.2:p.Ile655Val
CA123559
NM_004448.4:c.1963A>G