ClinGen Allele Registry
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Canonical Allele Identifier:
PA272924
Gene: MYH11
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000148691
RCV000182528
RCV000611174
RCV001174812
ClinVar Variation:
161316
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_074035.1:p.Arg1758Gln
CA084166
NM_022844.3:c.[5273G>A;4578+1G>T]
CA272923
NM_022844.3:c.5273G>A