Canonical Allele Identifier: PA658820196
Gene: GPR37L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 522590
ClinVar RCV Id: RCV000625728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004758.3:p.Lys349Asn
CA1330157
NM_004767.5:c.1047G>T
CA344235578
NM_004767.5:c.1047G>C