ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645495320
Gene: MYH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
225415
ClinVar RCV Id:
RCV000490432
RCV000455902
RCV001723786
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_060004.3:p.Val805Ala
CA8391132
NM_017534.6:c.2414T>C