Canonical Allele Identifier: PA2580275958
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087813
ClinVar RCV Id: RCV003009752
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Asp1925Asn
CA411371662
NM_002473.6:c.5773G>A