Canonical Allele Identifier: PA2580117558
Gene: HGF HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000592.3:p.Thr490Met
CA367873342
NM_000601.4:c.1469C>T