Canonical Allele Identifier: PA2741819114
Gene: HGF HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000592.3:p.Leu579Val
CA367872729
NM_000601.4:c.1735C>G