Canonical Allele Identifier: PA347311
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 204783
ClinVar RCV Id: RCV000192270 RCV000790360
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Asp1447Val
CA347309
NM_002473.6:c.4340A>T