Allele Registry

Canonical Allele Identifier: PA2830290037

Gene: SHMT1 HGNC NCBI

ClinVar RCV:

RCV000144920

ClinVar Variation:

157592

HGVS (amino-acid)	Matching Registered Transcripts
NP_683718.1:p.Leu435Phe	CA170988 NM_148918.3:c.1303C>T