Canonical Allele Identifier: PA2825303111
Gene: HGF HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001010932.1:p.Leu574Val
CA367872729
NM_001010932.3:c.1720C>G