Allele Registry

Canonical Allele Identifier: PA2573265921

Gene: SRRM2 HGNC NCBI

ClinVar RCV:

RCV002246851

ClinVar Variation:

1686338

HGVS (amino-acid)	Matching Registered Transcripts
NP_057417.3:p.Ser346Phe	CA7847145 NM_016333.4:c.1037C>T