Canonical Allele Identifier: PA204769
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208726
ClinVar RCV Id: RCV000190742 RCV001173632 RCV001224770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_612370.3:p.Pro707Leu
CA204767
NM_138361.5:c.2120C>T