ClinGen Allele Registry
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Canonical Allele Identifier:
PA096578
Gene: TMEM231
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
48421
ClinVar RCV:
RCV000033042
RCV000255979
RCV000543480
RCV002513311
RCV003155046
ClinVar Variation:
39822
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001070886.1:p.Asp209Asn
CA130593
NM_001077418.3:c.625G>A