Canonical Allele Identifier: PA2825303088
Gene: HGF HGNC NCBI

Linked Data

ClinVar Variation Id: 2195033
ClinVar RCV Id: RCV002637444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001010932.1:p.Thr485Met
CA367873342
NM_001010932.3:c.1454C>T