Canonical Allele Identifier: PA216322
Gene: SLC4A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64516
ClinVar RCV Id: RCV000054703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003031.3:p.Pro18Leu
CA216321
NM_003040.4:c.53C>T