ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829399141
Gene: MYH11
HGNC
NCBI
Linked Data
ClinVar Variation Id:
374963
ClinVar RCV Id:
RCV000415719
RCV000772071
RCV001555668
RCV001374827
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002465.1:p.Thr1911Met
CA7921155
NM_002474.3:c.5732C>T