Canonical Allele Identifier: PA2826144202
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 517313
ClinVar RCV Id: RCV000606613 RCV000851949 RCV000861598 RCV000660563 RCV000851887 RCV001270563 RCV002245051 RCV002280881 RCV003313786 RCV003403425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171670.1:p.Pro206Leu
CA3114629
NM_001184741.1:c.617C>T