Canonical Allele Identifier: CA14689618
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648308T= , CM000681.2:g.41648308T= GRCh38

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3194A=