ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA358279
Gene: MYPN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
31819
ClinVar RCV Id:
RCV000024512
RCV000206974
RCV000247848
RCV000216191
RCV000624690
RCV000852614
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001243196.1:p.Leu1161Ile
CA215338
NM_001256267.2:c.3481C>A