Canonical Allele Identifier: PA2828081060
Gene: VPS37A HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350098.1:p.Lys292Asn
CA213061
NM_001363169.1:c.876A>T
CA370405454
NM_001363169.1:c.876A>C