Canonical Allele Identifier: PA645294962
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 341492
ClinVar RCV Id: RCV000343175 RCV000392449 RCV003727702
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Thr1906Met
CA10208952
NM_002473.6:c.5717C>T