Canonical Allele Identifier: PA916029535
Gene: PDGFRA HGNC NCBI

Linked Data

ClinVar Variation Id: 459033
ClinVar RCV Id: RCV000560051 RCV001262590 RCV002258945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334757.1:p.Met667Ile
CA356893638
NM_001347828.2:c.2001G>A
CA356893639
NM_001347828.2:c.2001G>C
CA356893640
NM_001347828.2:c.2001G>T