ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA112531
Gene: MYPN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
31792
ClinVar RCV Id:
RCV000024485
RCV000043543
RCV000219549
RCV000621596
RCV003989299
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001243196.1:p.Val1195Met
CA143766
NM_001256267.2:c.3583G>A