Canonical Allele Identifier: PA239001
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193480
ClinVar RCV Id: RCV000173552 RCV000278067 RCV003947462 RCV004020059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542400.2:p.Pro8Ser
CA026503
NM_080669.6:c.22C>T