Canonical Allele Identifier: PA645427820
Gene: CA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 324231
ClinVar RCV Id: RCV000366585 RCV000757049 RCV003940282 RCV003888774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000708.1:p.Met139Leu
CA8685357
NM_000717.5:c.415A>T
CA400455852
NM_000717.5:c.415A>C