ClinGen Allele Registry
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Canonical Allele Identifier:
PA177071
Gene: MYH9
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
176256
ClinVar RCV:
RCV000151322
RCV000416222
RCV001150618
RCV001150619
RCV001375382
ClinVar Variation:
164421
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002464.1:p.Lys1676Glu
CA177069
NM_002473.6:c.5026A>G