Canonical Allele Identifier: PA2826005099
Gene: GFRA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 208201
ClinVar RCV Id: RCV000190397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158510.1:p.Ser137Phe
CA204399
NM_001165038.2:c.410C>T