Canonical Allele Identifier: PA2828937101
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 566097
ClinVar RCV Id: RCV000685827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371072.1:p.Asn412Lys
CA199849706
NM_001384143.1:c.1236C>A
CA374932501
NM_001384143.1:c.1236C>G